Scientist Jobs Near Me

We are looking for a *biology research scientist *to join our team to train AI models. You will measure the progress of these AI chatbots, evaluate their logic, and solve problems to improve the quality of each model. In this role you will need to hold an expert understanding of biology- a completed or in progress Masters/PhD is preferred but not required. Other related fields include, but are not limited to: Microbiology, Cell Biology, Genetics, Physiology, Biochemistry, Molecular Biology, Biotechnology, Environmental Science. Benefits: * This is a full-time or part-time REMOTE position * You'll be able to choose which projects you want to work on * You can work on your own schedule * Projects are paid hourly starting at $40+ USD per hour, with bonuses on high-quality and high-volume work Responsibilities: * Give AI chatbots diverse and complex biology problems and evaluate their outputs * Evaluate the quality produced by AI models for correctness and performance Qualifications: * A current, in progress, or completed Masters and/or PhD is preferred but not required * Fluency in English (native or bilingual level) * Detail-oriented * Proficient in biology and inductive/deductive reasoning, experimental design, data interpretation, and systems-level thinking. Note: Payment is made via PayPal. We will never ask for any money from you. #INDUSBIO Job Types: Full-time, Part-time Pay: From $40.00 per hour Benefits: * Flexible schedule Work Location: Remote

Genesis Research is an international healthcare consultancy providing value evidence strategy, generation, synthesis, and communication services to Life Sciences companies. Delivering these services empowered by technology innovations has enabled us to become a trusted partner with our clients across the development and commercialization life cycle. Combining both traditional and novel analytical approaches with diverse real-world data, including genomic, medical record, claims and patient-reported information, has allowed us to inform Life Science company internal decision making as well as submissions and presentations to regulators; health technology assessment authorities and payers; the medical community; and, patient organizations. We are looking for an experienced Principal Scientist to join our Analytics team. Accountabilities within this role: • Develop efficient and error-free code using SAS/R and SQL that accurately applies the methodologies defined to complete the analysis. • Produce and present client-ready tables and charts with strong aesthetics ready to present both internally and to clients by utilizing Excel & PowerPoint. • Contribute to the development and growth of protocols and statistical analysis plans by providing analytical, database, therapeutic, epidemiological, and statistical expertise and experience. • Design, implement and interpret basic & advanced statistical methods. • Working knowledge of multiple databases that are commonly utilized. • Conceptualize the scope of projects and time required from project initiation through completion of client deliverables. • Handle multiple concurrent projects/tasks and meet all internal and external deadlines by effectively managing one's own time. • Provide proactive, responsive, high quality execution of client deliverables. • Lead proposal development with oversight from client director, lead client meetings, assist with development of scientific communications (abstracts/posters). Qualifications: • Bachelor's degree in a technical or quantitative field from an accredited college or university (e.g., statistics/ biostatistics, epidemiology, bioinformatics, health economics, mathematics, outcomes research, public health, biology, medicine); Masters, MPH or PhD degree preferred. • 4+ years relevant work experience (less with PhD). • Demonstrated knowledge of R/SAS and statistical methods over a 6+ year period. • Experience developing and implementing statistical analysis plans utilizing RWD or clinical trials. • Demonstrated thorough aptitude for conducting quantitative and qualitative analyses. • Willingness to provide superior customer service through first-rate work product. • Ability to work independently and collaboratively. • Strong communication skills with the ability to explain technical data analysis results to business people, as well as communicate quantitative challenges and issues to technical people. Knowledge Preferred: • Significant experience working with analytical models and visualization techniques and tools. • Advanced analytics techniques (regression, simulation, etc.). • Identifying and addressing client needs, building relationships with clients, developing requests for proposals. • Creative and innovative problem solving skills. • Ability to work under tight deadlines in a highly dynamic environment. Compensation: Competitive salary Performance-related bonus Hybrid/Remote work environment Private insurance Flexible PTO plan and many company holidays including the last week of the year Genesis Research is an equal opportunity employer.

Kelly Science has and Immediate opening for a Scientist III, QC Labs for our growing client near Columbus, OH Shift: 2nd Full-time Direct Hire Salary: $75,000-$100,000 DOE Your Role: As a Scientist III, QC Labs, you will play a pivotal role in ensuring the highest standards of quality and regulatory compliance. You'll be responsible for conducting sophisticated testing of raw materials, active pharmaceutical ingredients (APIs), and finished products to ensure they meet both customer requirements and regulatory standards. You'll also contribute to the continuous improvement of analytical methods and troubleshooting, working closely with a collaborative team in a fast-paced and ever-evolving environment. Key Responsibilities: Perform Analytical Testing: Conduct qualitative and quantitative chemical and physical testing for APIs, starting materials, packaging components, and finished products, ensuring accuracy and regulatory compliance. Ensure Regulatory Compliance: Maintain adherence to current DPs, SOPs, and cGMP regulations while performing testing and documenting results. Documentation & Reporting: Maintain clear, organized records in laboratory notebooks, worksheets, and documents. Author detailed technical reports to improve analytical methods. Investigative & Troubleshooting Work: Apply advanced analytical techniques to resolve complex issues, investigate discrepancies, and ensure proper use of laboratory equipment. Collaborate with Cross-Functional Teams: Act as a key player in meetings with stakeholders to discuss laboratory deviations, lead troubleshooting efforts, and provide guidance to junior scientists. Review & Approve Analytical Data: Ensure all analytical documentation and batch records are reviewed, validated, and released in accordance with company procedures and specifications. Desired Analytical Expertise: For APIs: Proficiency in UV, HPLC, GC, UPLC, KF, FTIR, Advanced Data Review, Lead Investigator, and Disposition (Packaging/Labeling). For Pharmaceutical Products: Expertise in HPLC, UPLC, Chromatographic Data Systems (Empower preferred), Laboratory Information Management Systems (LabWare preferred), and Advanced Data Review. Additional Desired Techniques: Experience with particle size analysis, ICP, AA, viscosity, XRD, GC, IC, droplet size distribution, FTIR, and microscopy. What You Bring to the Team: A BS in Chemistry (or related science field) with a minimum of 5 years of GMP pharmaceutical analytical chemistry experience, or 10 years of relevant experience with a high school diploma. Hands-on experience executing and evaluating analytical methods for APIs and pharmaceutical products, including both compendial and non-compendial testing. Expertise in advanced analytical techniques, method troubleshooting, and data review. Strong ability to work independently and as part of a team to manage multiple projects simultaneously in a fast-paced environment. Exceptional written and verbal communication skills, including the ability to organize and lead meetings with stakeholders to discuss lab deviations. A collaborative mindset with the ability to mentor junior scientists in laboratory techniques and best practices. What We Offer: Competitive Compensation: Annual performance bonus, commission, and share potential. Comprehensive Benefits: Health, dental, vision, mental health, disability, life insurance, prescription drug coverage, and a variety of voluntary benefits. Generous Time Off: Starting with 20 days PTO (prorated), additional days at milestone anniversaries, 3 personal days, and 11 company-paid holidays. Retirement & Savings: Auto-enrollment in a Hikma-sponsored 401(k) with a 100% match on the first 6% of eligible pay you contribute. Wellbeing & Employee Discounts: Access to our Wellbeing Rewards Program and employee discount offerings. Career Growth: Career advancement opportunities and access to tuition reimbursement to further your education. Family Support: Paid maternity and parental leave to support you during important life milestones. Why Join Us? We value your expertise and dedication. Here, your contributions matter. Join a company that prioritizes safety, quality, and growth. Together, we will innovate, improve, and make a lasting difference in the pharmaceutical industry. Ready to take your career to the next level? Apply now!

BASIC FUNCTION: Omya Technology Center at Cincinnati (OTCC) is looking for a talented, hardworking, inquisitive minded and resourceful Associate Scientist with unique knowledge in the areas of analytical techniques for inorganic and organic materials, glass microsphere production and characterization, glass and ceramic science, test validation and qualification (both with internal and external customers), and data mining. In addition, to ensure that technical service, sales and manufacturing teams receive accurate and timely laboratory support needed to increase sales and/or overcome manufacturing challenges. Provide laboratory leadership for technicians and associate scientists. RESPONSIBILITIES: Interact with other company functions to assist in determining the greatest technical and marketing needs of the organization. Bring ideas to innovation using lean innovation processes to create, select, and commercialize those ideas as fast as possible. Lead and direct laboratory projects, utilizing design of experiments and the scientific method, to address these needs (e.g. customer technical issues or production challenges). Write quality reports detailing the problem, procedure, results and conclusions; educate other laboratory employees by sharing and discussing these projects/reports with them. Provide training, as needed, to less experienced personnel. Perform analyses as needed to expedite testing. Conduct research on perlite, zeolite, and other minerals or products containing silica to increase knowledge of the product and its associated technologies for LWF. Excellent communication, multitasking, and organization skills. Demonstrated hands on research skills. Show expertise with several analytical methods and industry specific processing methods. Assist in the maintenance, calibration and troubleshooting of laboratory equipment. Develop and modify methods and equipment in a safe manner, as needed, to address relevant technical issues. Assist technicians, as needed, to complete testing/experiments in a timely fashion. Familiarity with literature and patent search using multiple tools. QUALIFICATIONS: Bachelor's degree in chemistry, material science, chemical engineering, or another related field. Master's Degree or MBA is a plus. Minimum of 1 - 5 years' technical experience. Experience with application testing. Expertise on light weight fillers materials and applications is a plus. An innovative and flexible mindset with high regard to safety is a must. Understand mathematical and statistical techniques relevant to product testing. Develop a solid understanding of products and applications to provide direction to the team and support project work. Work in an ISO-certified environment. Must possess current US employment authorization. Sponsorship not available for this position. EOE

The Associate Research Chemist will perform a broad range of chemical tests and procedures in the laboratory using professional judgment in the evaluation, selection, and adaptation of professional methods and techniques. CORE & ESSENTIAL FUNCTIONS: Provides service and testing assistance to laboratory department management, utilizing professional chemical background and accepted industry procedures and techniques in line with company policy requirements. Perform bench blending and testing Writes technical and laboratory reporting for projects Completes company-required forms in connection with project assignment Presents completed reports verbally, if requested, to department director Review American Society for Testing and Materials (ASTM) procedures and perform follow-up testing pursuant to ASTM protocols Other duties as assigned QUALIFICATIONS AND SKILLS: Bachelor of Science degree in Chemistry or Chemical Engineering and 1 year of relevant industry experience preferred. Experience with laboratory equipment use and procedures with a respect for safety. Working knowledge of thermoplastic compounds, testing, processing and development. Knowledge of sealants, adhesives, and coatings testing and formulating is preferred. Prior experience with bitumen based technology is a plus. Demonstrated aptitude for problem-solving; ability to determine solutions for customers. Excellent communication and organizational skills. The ability to learn new concepts/procedures quickly. Adherence to health and safety regulations (e.g. use of protective gear). Must be results-orientated and able to work both independently and within a team environment. Must possess excellent verbal and written communication skills. Proficiency in using Microsoft Office Suite applications. PHYSICAL REQUIREMENTS: Ability to communicate orally in a clear, concise and effective manner with the customers, account representatives, company representatives, management, staff, and the public in face-to-face, one-on-one and group settings. Ability to use a telephone for communication. Ability to maintain regular, predictable, and punctual attendance at the facility. Ability to establish and maintain effective working relationships with others. Use office equipment such as a personal computer, copier and facsimile machines. Ability to communicate in writing in a clear, concise and effective manner. Sit, stand and/or walk for extended time periods. Hearing and vision required to be within normal ranges. Ability to accurately distinguish color variation. Read at, above, and below shoulder height. Occasionally stoop, kneel or crouch. Sufficient manual dexterity required to operate equipment. Tolerate inclement weather, including heat and cold. Normal range of tolerance to household and other types of typical industrial/construction chemicals and solvents. EQUAL OPPORTUNITY EMPLOYER: The Garland Company, Inc. is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, sex, color, religion, national origin, ancestry, military status, veteran status, marital status, gender identity or expression, transgender status, citizenship, sexual orientation, age (40 and older), disability (except where the disability prevents the individual from being able to perform the essential functions of the job and cannot be reasonably accommodated) or any other legally protected characteristic under federal, state or local law.

Leonardo.Ai seeks a Senior Research Scientist to join our expanding global AI team. We're advancing our generative AI platform to empower millions, regardless of expertise, with intuitive tools for creating high-quality images and videos. Now part of Canva, we're ready to build a world-class R&D team to seamlessly integrate AI products, tools, and features, making creativity limitless for nearly a quarter of a billion users. The Role: As a Senior Researcher, you will play a pivotal role in building and training new foundational models as we advance further into image, video, 3D, and language modelling. We are working at the cutting edge of what's possible and pushing every day to go beyond it. Responsibilities: Lead Multimodal Research: Spearhead research in multimodal AI, including image, video, 3D, and language modelling. Drive cross-modal innovation to address complex challenges across media types. Foundational Model Development: Architect, train, and evaluate foundational models. Research and Application: Work in exploratory phases to gain new insights and apply them to improving model outcomes. Skills we love you to have: Multimodal AI Expertise: Experience in text-to-image, video comprehension and synthesis, 3D generation, with knowledge of training LLMs for multimodal applications. Foundational Model Building and GPU Proficiency: Skill in building foundational models from scratch, leveraging GPU technology for performance and scaling. Advanced Model Architectures: Background in GANs, transformers, and diffusion models, especially for multimodal applications, keeping up with industry advancements. Academic and Open-Source Contributions: Record of peer-reviewed publications and contributions to open-source projects. Technical Proficiency: Expertise in Python, frameworks such as PyTorch or Jax, and cloud computing. Collaborative Attitude: Strong team player experienced in cross-functional collaboration. Competitive Edge: Stay ahead of industry trends with AI-based literature, competitors, and emerging technologies. Help maintain our competitive edge in the market by providing insights and recommendations. Educational Background: PhD or Master's in AI or similar field with proven research experience. Our Culture: Inclusive Culture: We celebrate diversity and are committed to creating an inclusive environment where everyone feels valued and empowered. Flexible Work Environment: We understand the importance of work-life balance. Enjoy the flexibility to work remotely or from our vibrant offices. Empowering Growth: Your development is our priority. We offer continuous learning opportunities and career growth tailored to your goals. Impactful Work: Join us in shaping the future of AI. You'll work on innovative projects that have a meaningful impact. Next Steps: If you're passionate about AI research and have a history of implementing AI models, this role might be the perfect fit for you. We encourage you to apply and start the conversation whether you're based locally in the USA or overseas. Why Leonardo.Ai? Shape the Future of AI: Join us in revolutionising content creation and build a platform at the forefront of generative AI. Hybrid and Remote Options: Flexibility is key. Choose a work arrangement that suits your lifestyle. Benefits: We offer a generous package including paid parental leave and a wellness budget. Diversity and Inclusion: We intentionally seek people from a variety of backgrounds to join our team. Typical Interview Process While we love technology, our interview process is all human. A Talent team member will review your application, and we'll contact you either way. Here's what you can expect: Round 1 - Meet Your Recruiter: Our Talent team will arrange a 30-minute video call to discuss your experience and the role. Round 2 - Craft Interview: You'll meet team members to discuss the technical task and your expertise. Round 3 - Technical Task: You may be given a short take-home task to assess your skills. Round 4 - Values Interview: You'll meet with the Department Head for a conversation about your potential impact. Important Information If there are any adjustments we can make to make you more comfortable at any point in the interview process, please let us know. #J-18808-Ljbffr

COLTENE is a global leader in the development, manufacture and sale of consumables and small equipment for dental treatment applications. COLTENE operates production facilities in Switzerland, Germany, Canada, France and the USA, as well as a worldwide sales network with its own representatives and distribution partners. Dentists and dental technicians worldwide rely on COLTENE products, both for conventional, as well as implant-based treatment and dental reconstruction. We are looking for a Product Engineer to joing our R&D Team in Cuyahoga Falls, OH site. Product Engineer shall support the product portfolio, customer needs and P&L objectives of Coltene by contributing to all phases of the product lifecycle as required. Adherence to domestic and international regulations and local design control practices will be of critical importance for all work performed. Duties and responsibilities Participate in cross-functional teams for both small and large projects. Generate new ideas or technologies which can be applied to new products. These concepts can be developed into initial designs and the coordination of activities to generate design prototypes for testing. Evaluate and select appropriate materials for product designs, considering factors such as mechanical properties, cost, manufacturability, and environmental impact. Optimize material usage to enhance product performance and reduce costs. Create and execute test procedures, including documentation of procedures, recording of results and generation of reports. Testing to perform verification and validation must meet regulatory guidelines. Assemble required documentation to transfer new product designs to production. Evaluate product issues and defects based on customer or manufacturing complaints. Identify root cause and develop and implement design-related corrective action plans per quality standards. Create innovative solutions to existing products in the areas of quality, cost, or functionality as needed. Analyze and evaluate design activities, including the analysis of materials, stresses, dimensions, tolerances, manufacturability, and satisfaction of design input requirements. Create and maintain product specifications, including 3-D CAD models of parts and assemblies, electrical schematics, layouts, parts lists and cost estimates. Provide direction to Engineering Services in the creation of detailed drawings and specification documents. Adhere to Coltene Design Control procedures and all applicable regulatory guidelines when working with product designs. Maintain project and product documentation in accordance with GMPs, FDA, ISO, MDR and other pertinent regulatory governance, including Design History Files, Technical Documentation, User Guides and Technical Repair Manuals. Assist Marketing and/or Regulatory team members in the development of product labeling and literature by recording, interpreting and explaining technical data and product performance. Maintain documents included in a risk management file, including Hazard Analyses, Risk Analyses, and dFMEAs. Communicate with internal and external manufacturers regarding product design, quality and manufacturing-related issues. Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice. Qualifications The minimum qualifications listed below are representative of the knowledge, skill and/or ability needed to successfully perform the job. Bachelor's degree in engineering or other technology field required (Mechanical Engineering/Material Science strongly preferred) 6+ years of progressive experience successfully leading new product development projects Familiarity with medical device standards preferred (ISO 13485, IEC 60601-1, ISO 10993, 21 CFR Part 820, etc.) Proficient in 2D/3D CAD design software (Autodesk Inventor preferred) Proficient in Microsoft Office Suite (Teams, Word, Excel, Project, Visio, Power Point, Outlook, etc.) Able to provide guidance and mentoring to team members when appropriate Able to adapt to and adopt new technologies. Able to apply technical knowledge to think critically solve problems, and analyze Able to assess situations and make logical decisions, communicate in a timely manner (both verbal and written) and report effectively to internal and external audiences. Able to manage time effectively Comfortable taking initiative independently Working conditions While performing the duties of this job, the employee works in both an office and plant environment. While in the plant, the employee regularly works near moving mechanical parts. The noise level in the work environment is quiet to moderate. This is a full-time exempt position requiring at least 40 hours per week, with hours of work and days scheduled determined by the Research & Development Manager. Special circumstances such as off shift and weekend work might occur on rare occasions.This position requires minimal travel. Potential for remote/hybrid work arrangement exists on a discretionary basis. Physical and non-physical requirements While performing the duties of this job, the employee spends time sitting at a desk, however the employee is frequently required to stand for periods of time and work out in the manufacturing area on projects.Prolonged periods of concentration and focus are required along with adequate interpersonal skills and the ability to deal with stress of time constraints. The employee is occasionally required to use hands and fingers to handle, or feel objects, tools or controls; reach with hands and arms; and talk or hear. The employee must occasionally lift and/or move up to 50 pounds. This position requires regular and consistent attendance. Direct reports None Benefits Coltene offers a comprehensive employee benefit program that enables our employees to stay healthy, feel secure and maintain a work/life balance: Generous Paid Time Off | Holiday Pay | Medical/Prescription Insurance | Dental Insurance | Vision Insurance | Health Savings Account (HSA) | Company-Paid Life and AD+D Insurance | Company-Paid Long-term and Short-term Disability | Voluntary Life Insurance | Voluntary Critical Illness, Hospital and Accidental Injury Insurance | 401(k) | Tuition Reimbursement Program EOE STATEMENT It is the policy of Coltene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Coltene will provide reasonable accommodations for qualified individuals with disabilities.

Primer exists to make the world a safer place. We do this by providing trusted decision-ready AI to the world's most critical organizations. Our software enables leaders, operators, and analysts to better understand the changing world around us in real time and make informed decisions when the stakes are high. Primer has offices in San Francisco, Pasadena, CA, and Arlington, VA. For more information, please visit primer.ai. As a Staff Machine Learning Research Scientist, you will work on some of the deepest problems in machine learning. You will publish papers, attend conferences, and file patents. But you will also ship code right into the products used every day. We call it applied research, and you will be one of the leaders, taking part in a thriving team of engineers whose backgrounds span computer science to particle physics. You will be constantly learning and mentoring, keeping Primer at the leading edge of the most important technology today. Roles and Responsibilities - How You Will Make an Impact Track and understand the machine learning research landscape Help us make the strategic technology investments that ensure Primer's leadership in the space Design, lead, and review experimental work Collaborate and influence cross-functional teams to drive our technology roadmap Lead and mentor data scientists to help them grow Improve and promote best practices across the company and motivate others to follow your high standard Relevant Skills and Experience Graduate degree in computer science or related field 5+ years in machine learning with a focus on machine learning research Demonstrated track record of publications and/or open source projects Hands-on experience with machine learning and NLP tools and libraries from Numpy to PyTorch Curiosity, enthusiasm, and a love for teaching and learning Compensation and Employment Conditions The annual cash compensation range for this position is US$180,000 to US$250,000. Final compensation will be determined based on experience and skills and may vary from the range listed above. This role will consider applicants out of San Francisco, CA or Washington, DC. Primer works closely with the U.S. defense and intelligence establishment. Any offer of employment is conditioned on an applicant or employee being able to meet any applicable government contract requirements. What We Offer We are a series D funded company with investors from Addition, USIT, Lux Capital, Amplify Partners, Addition Capital, Bloomberg Beta, and others. We are intentional about building a diverse and inclusive team of subject matter experts to better advocate for the needs of our users. We care a lot about our work and the well-being of our team. We encourage everyone to work at a sustainable pace and have a flexible vacation policy for team members to utilize, Wellness Days, and 100% paid leave for parents of growing families. We offer competitive compensation and comprehensive benefits. This includes full medical, dental, and vision coverage, fertility benefits through Carrot, mental health coverage on demand with Headspace Care+, Gympass+ Membership via Wellhub, One Medical Membership, 401(k), remote work stipends, and monthly internet allowance. Primer is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. If you need assistance or accommodation due to a disability, you may contact us at ***************. Pursuant to the San Francisco Fair Chance Ordinance, we will consider for employment qualified applicants with arrest and conviction records. Apply for this job * indicates a required field First Name * Last Name * Email * Phone * Resume/CV * LinkedIn Profile Website Are you legally authorized to work in the United States? * Select... Will you now or in future require sponsorship for employment visa status (e.g., H-1B, F-1, or TN visa status)? * Select... Do you have a U.S. Security Clearance? * #J-18808-Ljbffr

The Organization What's happening at Entrada Therapeutics? Entrada is a clinical-stage biopharmaceutical company aiming to transform the lives of patients by establishing a new class of medicines that engage intracellular targets that have long been considered inaccessible. Our Endosomal Escape Vehicle (EEV)-therapeutics are designed to enable the efficient intracellular delivery of a wide range of therapeutics into a variety of organs and tissues, resulting in an improved therapeutic index. Through this proprietary, versatile and modular approach, Entrada is advancing a robust development portfolio of RNA-, antibody- and enzyme-based programs for the potential treatment of neuromuscular, ocular, metabolic and immunological diseases, among others. Our lead oligonucleotide programs are in development for the potential treatment of people living with Duchenne who are exon 44, 45 and 50 skipping amenable. We have also partnered to develop a clinical-stage program, VX-670, for myotonic dystrophy type 1. We are a tight-knit team of experts and leaders in both therapeutic development and rare diseases and are excited to grow and attract colleagues who are ready to join a high-energy, dedicated team that likes to get things done and dramatically improve the lives of patients and their families. The Perfect Addition to Our Team You are a highly motivated, collaborative, and innovative Drug Metabolism and Pharmacokinetics expert with experience driving preclinical DMPK activities. We have a diverse pipeline and as such you should have experience across both small and large molecules and have hands on experience leading the design, analysis, and interpretation of preclinical in vitro and in vivo studies. You are an exceptional communicator and a natural collaborator who is excited about the opportunity to contribute to this function and work closely with cross functional leaders. The Opportunity The ideal candidate will serve as a subject matter expert working within the DMPK team to drive the DMPK strategy across all designated programs and pipelines. They will have the opportunity to design, manage, and execute DMPK deliverables, and will be responsible for analyzing, interpreting, and authoring/reviewing ADME and PK/PD reports. Responsibilities Lead all PK- and ADME-related efforts for designated program(s). Communicate and present relevant information across all areas of the organization, regardless of level. Select and manage PK/TK, PK/PD, and ADME CROs. Author and review PK/TK, PK/PD, and ADME reports. Author and review relevant PK/TK, PK/PD, and ADME sections of regulatory submission documents (e.g. investigational new drug (IND), investigator brochure (IB), clinical trial application (CTA), etc). Review associated reports, including clinical, toxicology, pharmacology, and bioanalysis. Collaborate with clinical teams, including pharmacology, biomarkers, development, and operations. Collaborate with non-clinical development teams, including toxicology and bioanalysis. Collaborate with discovery teams to guide future programs and better understand mechanisms of action. This is a US based remote position, with preference given to local New England based candidates. This role will require minimum monthly or quarterly travel to the Entrada Therapeutics Headquarters located in Boston, MA. The Necessities At Entrada, our passion for science, our devotion to patients and our values drives our behavior: Humanity - We genuinely care about patients and about one another. Tenacity - We are relentless and persistent in the pursuit of developing therapies for patients. Creativity - We are creative problem solvers. Collaboration - We are more than the sum of our parts. Curiosity - We have a growth mindset and push conventional thought and theory. To thrive on our team, you will need to come with: PhD in pharmacology or similar field with 8+ years of DMPK experience in an industry setting or a MS with 12+ years of relevant experience. Expertise with ADME studies and assays, with a proven track record of strategizing and troubleshooting based upon raw data. Vendor Management experience, specifically managing CROs. Additional experience with other aspects of ADME, bioanalytical techniques, PK/PD, toxicokinetics, pre-clinical PK/PD modeling, and translational biology are strongly preferred. Experience with oligonucleotide-based modalities. Experience authoring and reviewing DMPK-related reports and regulatory documents for health authority submissions is highly desirable. You should be naturally collaborative and a strong communicator, and let's not forget the ability to multi-task effectively and work within aggressive timelines- these are key to being successful in Entrada's fast paced environment. The Perks By becoming a team member here at Entrada, you'll have access to competitive health, dental, and vision coverage, as well as life insurance, and short term and long-term disability insurance. We value work life balance, you'll benefit from discretionary time off, paternity leave, and an excellent 401(k) package. We also offer a generous transportation stipend to commute as you wish. Our location in the vibrant and growing Seaport District is close to all the best that the city of Boston has to offer. Entrada Therapeutics is an equal opportunity employer. Qualified candidates will receive consideration for employment without regard to race, color, religion, national origin, gender, sexual orientation, gender identity or expression, age, mental or physical disability, and genetic information, marital status, citizenship status, military status, protected veteran status or any other category protected by law. #J-18808-Ljbffr

Staff Data Scientist - Transform Work Travel with AI & Machine Learning $200,000 to $230,000 base salary Fully remote (The company is SF based) Are you ready to shape the future of work travel? We're a fast-growing, well-funded travel technology company that's redefining how businesses and teams experience travel. Our cutting-edge platform simplifies booking, billing, and trip modifications, creating a seamless experience backed by AI-driven insights. The Role: As a Senior Data Scientist, you'll drive the development and optimization of key machine learning models and data-driven strategies. Your work will directly impact business decisions, product enhancements, and customer experiences. Responsibilities: Develop and implement ML models for lead scoring, churn prediction, pricing optimization, personalization, and fraud detection. Collaborate with engineering and business teams to turn insights into actionable strategies. Lead end-to-end data science projects, from data collection to model deployment and monitoring. Work alongside data infrastructure and analytics teams to enhance data capabilities. Clearly communicate technical findings to non-technical stakeholders. What they are looking for: 5+ years of industry experience in data science or machine learning engineering. Strong expertise in ML algorithms, statistical modeling, Python (scikit-learn, numpy, pandas), and SQL. Experience with Snowflake and Streamlit is a plus. MS/PhD in Mathematics, Statistics, Operations Research, Economics, Engineering, or Computer Science. Problem-solving mindset with a focus on simple, effective solutions. Ability to thrive in a fast-paced, high-growth environment. What they Offer: Competitive compensation, including salary, bonuses, and equity opportunities. A hybrid/remote-friendly work environment with resources tailored for success. Comprehensive benefits and a strong culture of innovation and collaboration.

We are looking for a highly motivated and independent new graduate from a top university to join our team as an AI Research Associate. In this role, you will conduct research on AI market trends, evaluate product opportunities, perform investment due diligence, and contribute to various aspects of AI-related projects. You will also manage relationships with AI founders, source deals, assist with AI product development, and help organize AI events. You will work closely with a diverse, cross-border team. Previous experience with AI is a plus, but strong analytical skills, high agency, and the ability to work independently are critical for success in this role. Location: Remote (Silicon Valley preferred, or willing to travel) Key Responsibilities Conduct in-depth research on AI technologies, products, and market opportunities Evaluate and perform due diligence on investment opportunities Deal sourcing for AI projects and startups Manage relationships with AI founders and key stakeholders Contribute to AI product development and strategic planning Assist with the planning and execution of AI-related events Analyze reports and summarize key findings for team discussion Work closely with a multi-cultural, cross-border team to identify strategic insights Stay updated on the latest AI trends and innovations Contribute to internal discussions and strategic decisions Qualifications Recent graduate from a top university (preferably in AI, Engineering, or a related field) Strong research and analytical skills Ability to work independently with minimal supervision Comfortable working in a multi-cultural, cross-border team Familiarity with AI technologies and market trends (preferred) Proficiency in English (for Chinese candidates, English proficiency is required) Ability to travel to Silicon Valley if based remotely High agency and a proactive mindset Excellent written and verbal communication skills Additional Desired Qualities: Familiarity with AI startup ecosystems Passion for AI and emerging technologies Comfort with remote work and self-driven projects Ability to adapt to fast-paced, dynamic work environments What's In It For You? Join a diverse team of talented individuals who are passionate about growth and innovation. Opportunities for personal and professional development. Be part of our expansion plan and contribute to our global success. Engage in cross-functional teamwork through international events and retreats.

Join us as we pursue our disruptive new vision to make machine data accessible, usable and valuable to everyone. We are a company filled with people who are passionate about our product and seek to deliver the best experience for our customers. At Splunk, we're committed to our work, customers, having fun and most importantly to each other's success. Learn more about Splunk careers and how you can become a part of our journey! Role: As the Principal Applied Scientist in the Artificial Intelligence group, you will be responsible for developing the core AI/ML capabilities to power the entire Splunk product portfolio and help our customers to drive their journey to digital resiliency. You will collaborate with cross-functional teams, mentor junior team members, and help drive the scientific roadmap of the area. Responsibilities: The responsibilities of this role include: Lead the development of core AI/ML models and algorithms that drive our product's key use cases in the cybersecurity and observability domains. Collaborate closely with software engineers, data scientists, and product managers to integrate generative AI solutions into our products and services. Stay up to date with the latest research and developments in the field of AI/ML, and ensure that these advancements are properly incorporated into our technology roadmap. Provide technical guidance and mentorship to team members to ensure the development of their skills. Actively participate in cross-functional discussions and strategic decisions related to AI research directions and product roadmaps. Requirements: Knowledge, Skills, and Abilities: PhD in Computer Science or a related field with at least 4 years of experience OR MS in Computer Science or related field with at least 7 years of industry experience. Deep understanding of ML frameworks (e.g., TensorFlow, PyTorch) and programming languages commonly used in AI research. In-depth knowledge and proven track record in AI/ML technology, including deep learning, time series modeling, natural language processing, and unsupervised learning. In-depth knowledge and proven track record in Generative AI technology and Large Language Models (LLM). Experience developing large-scale, complex models and deploying them in production systems. Strong problem-solving skills and the ability to translate research insights into practical solutions that address real-world challenges. Excellent communication skills with the ability to articulate complex technical concepts to both technical and non-technical audiences. Experience in mentoring and guiding junior researchers or team members. Experience in the Cybersecurity and/or Observability industry is preferred. Splunk, a Cisco company, is an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation, national origin, genetic information, age, disability, veteran status, or any other legally protected basis. #J-18808-Ljbffr

Dr. Mitchel Stacy Lab A postdoctoral research position is immediately available within the Center for Regenerative Medicine at Nationwide Children's Hospital working in the lab of Dr. Mitchel Stacy. Read more about the lab at the link below: Stacy Lab | Nationwide Children's Hospital Research in the lab is focused on the development and validation of quantitative imaging techniques that allow for characterization of cardiovascular diseases and vascular remodeling. Of particular interest is PET imaging of skeletal muscle perfusion and PET-based molecular imaging of vascular biology. The lab utilizes multiple imaging modalities, which include clinical and micro PET/CT, CT angiography, and ultrasound. The lab is equipped with a variety of image processing workstations, which include dedicated software for PET/CT image analysis, ANSYS for computational modeling research, dedicated tools for ultrasound image analysis, and a dedicated angiography workstation. Experimental work and training will be focused on pre-clinical models of vascular disease (small and large animal) and clinical cardiovascular imaging. Clinical imaging projects will be conducted in collaboration with The Ohio State University College of Medicine and additional pediatric hospitals across the United States. Candidates should be highly motivated with an interest in biomedical imaging, vascular biology, and/or skeletal muscle biology. Also required are excellent written and verbal communication skills, as the position will involve participation in manuscript and grant writing. For more information related to the lab's research, please refer to a list of recent publications... ********************************************************************** Keywords PET imaging Biomedical imaging Vascular Biology Cardiovascular Disease Nuclear Medicine Skeletal Muscle Biology Job Duties: Performing pre-clinical and clinical imaging experiments Design and conduct scientific experiments to obtain data Write and publish scientific manuscripts and journals Contribute to grant submissions for external funding Qualifications: Ph.D. or M.D. in Physiology, Biomedical Engineering/Sciences, or related field Desire to pursue a career in biomedical imaging and/or vascular surgery research Appropriate knowledge base and/or skills related to the topic area Good writing and verbal communication skills

Join our team to innovate and improve products designed to seal and protect global, concrete infrastructure. Supporting our commitment to quality products, our newly renovated laboratory hosts state-of-the-art equipment to support our research and development team. Join us in developing technology for today and tomorrow! Role Overview: As part of our research and development team you will: develop new products, support existing products, and provide technical support to production and the field. You will be testing products to industry standards, while also having the opportunity to influence standards and specifications within our industry. Production support includes scale-up new products and setting and maintaining quality assurance measures throughout the production process. This role reports to the Research and Development Director. Qualifications: Physical and Testing Laboratory experience preferred (3-7 years preferable). Ability to plan, organize and execute your own tasks for product development and technical support to meet company requirements. Broad understanding of production equipment and testing methodology required. Ability to prepare test reports utilizing Microsoft Word, PowerPoint, and Excel. Bachelor (BA or BS) degree in a science-related field of study such as Chemistry, Polymer Science or Material Science. Appropriate industrial experience in a related field without a degree will be considered on a case-by-case basis. Accountabilities: · Project Planning: Can independently plan and manage projects related to technical assignments with limited supervision. Responsible for plan containing objectives and target dates for completion of key activities.Summarizes conclusions in a concise and logical manner. · Project Activities: Develops laboratory plan for project experiments. Responsible for monitoring and completing the plan. Some supervision still required to ensure plan is consistent with long term goals and objectives. · Communication: Writes well-organized status and completion reports and can present timely and accurate project updates to a diverse audience as needed. Effective verbal and written skills are mandatory. · Technical Awareness/Growth: Maintains knowledge skill set in technical area(s) of focus and training. Can be called upon as an expert in limited situations by management to resolve problems or accomplish project activities. Must demonstrate intellectual curiosity in company's area of technology. · Problem Solving Ability: Solves problems in area of expertise with minimal management direction; can solve some problems in other business areas with appropriate direction. · General Laboratory Support: Assists in the development of applicable test methods to characterize existing or experimental products. Makes recommendation to lab management regarding purchase of lab and production equipment. · External/Internal Relations: Works well within technical and business groups to achieve company objectives as team member. Has established strong external contacts to improve project development and for personal growth. Participates in interdisciplinary project teams with minimal, if any, management guidance. · Patents and Publications: Demonstrates the ability to develop patentable technology and products if assignments permit. · Supervision/Leadership: Can supervise and train technicians and college interns when called upon. · Laboratory Safety: Supports company policies and procedures to achieve a zero accident and injury rate for the laboratory. About Concrete Sealants (ConSeal): Celebrating its 55 th anniversary in 2025, ConSeal leads the sealant industry through innovation, technical expertise and customer support to the precast concrete and concrete infrastructure industry. Our on-going commitment to the development of - often revolutionary - new products, coupled with our excellent technical and customer service support, has made us the one company users look to for the most reliable solutions to their concrete problems. Our products seal, coat, waterproof, densify and protect concrete with a growing array of potential solutions. Join us as we work side-by-side with concrete producers to provide the next industry innovation!

Inuvo, Inc. (NYSE American: INUV) is an Artificial Intelligence based technology company that designs, develops, and patents proprietary advertising solutions that it sells through agencies, directly to brands, and integrated into advertising platforms. Inuvo is seeking a highly skilled and motivated Machine Learning Engineer / Data Scientist to join our team. The ideal candidate is a problem solver, detail-oriented, and committed to delivering high-quality solutions. This role requires expertise in data analysis, machine learning, and algorithm design. The ideal candidate needs to have development experience. Candidates should thrive both independently and in collaborative, small-team environments. Salary range for this position: $100-$140k. Primary Responsibilities: Serve as a member of the Data Science and Machine Learning team, reporting directly to the Director of Data Science. Design, implement, and deploy high-performance, scalable machine learning algorithms. Develop and enhance large-scale data analytics tools and frameworks. Drive innovation by exploring and applying cutting-edge machine learning and data science methodologies. Requirements Ph.D. in Computer Science, Statistics, Engineering, or a related technical field. At least 3 years of software development experience in Java or Python. Minimum 3 years of experience in machine learning, data science, algorithm design, and large-scale statistical analysis. Proficiency in large-scale data processing tools such as Spark or Hadoop. Experience with Large Language Models (LLMs) and Natural Language Processing (NLP) is highly desirable. Strong understanding of data structure optimization and algorithm scalability. Familiarity with AWS and its suite of data analytics/ML tools is a plus. Knowledge of Kafka, Hive, SQL, and shell scripting is an added advantage. Proven track record of working on complex, modular projects with the ability to define designs and test scenarios independently. Strong curiosity and enthusiasm for data exploration and discovery. Proficient in verbal and visual storytelling with data to communicate insights effectively. US work authorization. What We Offer A collaborative and supportive work environment with opportunities to lead and innovate. Engagement in impactful projects with cutting-edge technologies. Opportunities for continuous learning and career growth. Inuvo Benefits Competitive health benefits, including medical, vision, dental, and various voluntary benefits. Flexible vacation, holiday, and sick leave. 401(k) Plan with company matching. Offer a hybrid of in-office and remote work. Inuvo is an Equal Opportunity Employer and seeks to foster community, inclusion, and diversity within the organization. We encourage all qualified candidates, regardless of racial, religious, sexual, or gender identity, to apply. #J-18808-Ljbffr

Xerion Advanced Battery Corp., a privately-held lithium-ion battery start-up, is commercializing its patented molten salt electroplating technology and battery architecture that together significantly enhances the performance of lithium-ion batteries while dramatically reducing manufacturing costs. In addition, our sustainable manufacturing process has much lower carbon emissions than the conventional process. We have an immediate opening for a cathode materials scientist. In this role, you will explore synthesis of LIB cathode materials using various methods. You will study LIB cathode materials using advanced characterization tools and communicate with the management team to facilitate team decision making. The successful candidate should have exceptional technical capability, communication, and project management skills. Prior experience in developing high Ni content cathode material is highly desired. Expertise in molten salts, chemical synthesis, electroplating, and/or batteries is a strong plus. This is a unique opportunity to join a well-funded, fast growing battery startup company. Your vision and expertise will help shape the future of the company and together we will make the world cleaner and more energy efficient! Responsibilities: · In charge of battery cathode materials development projects. · Summarize and report findings to the management team in a timely manner. · Conduct battery materials synthesis using methods including but not limited to: electroplating, solid-state, sol-gel, and molten salt synthesis. · Conduct battery materials characterization using tools including but not limited to: XRD, SEM, EDS, FTIR, Raman, and electrochemical methods. · Establish high quality SOPs. · Collaborate with academic and industrial partners in R&D projects. Requirements: · Research experience in battery materials, especially in materials synthesis and characterization. · Master degree with three years' experience in a battery company or Ph.D. degree in a related field. Xerion is located in Kettering, OH. If you are interested in the position, please reach out to us with a copy of your resume. Dr. Heng Yang, Director of R&D Xerion Advanced Battery Corp. Email: *************************** Phone: ************

Environmental Scientists Client: Large State Client Duration: 6 mo contract (very likely to extend, long term contract) Benefits: Health, Dental, Vision, PTO, Sick Days, 401k Schedule: Monday - Friday, 37.5-hour workweek (flexible based on fieldwork demands) About the Opportunity: The Department of Environment and Conservation (TDEC) is growing its team across five Environmental Field Offices. We're seeking 8 passionate Environmental Scientists to help protect Tennessee's natural resources through field-based environmental inspections, reporting, and compliance support. This is an excellent opportunity for recent science graduates or early-career professionals who enjoy working outdoors and solving problems in the field often thrive in this role. What You'll Do: Perform on-site environmental inspections-up to 80% of the role will be in the field Investigate illegal sewage discharges, water quality violations, water wells, and fish kills Conduct field sampling (e.g., water testing for E. coli and other contaminants) Apply and interpret environmental regulations including SSDS, SOPs, and NPDES permits Prepare accurate reports, inspection documentation, and digital records Engage with residents, local contractors, and agencies-communication is key Be on-call on occasion and travel locally to sites (mileage reimbursed) What We're Looking For: Bachelor's degree in Environmental Science, Biology, Chemistry, Agronomy, Soil Science, Hydrology, or related field Hands-on exposure (coursework, internship, or job) to topics like wastewater, biodiversity, soil mechanics, water sampling, or environmental regulation Working knowledge or willingness to learn: SSDS (Subsurface Sewage Disposal Systems) Standard Operating Procedures (SOPs) NPDES (National Pollutant Discharge Elimination System) Strong interpersonal skills - this is a highly collaborative and public-facing role Comfortable working outdoors in variable weather conditions and terrain Reliable transportation for local site visits (mileage reimbursed) Who Will Succeed: Someone who loves the outdoors and doesn't want to be behind a desk all day A candidate with a lab or scientific background looking to pivot to the field A personable, self-motivated individual who's not afraid to get their hands dirty Someone fresh out of college with relevant coursework or an internship and a strong drive to learn Individuals with backgrounds in agriculture, service industry, or environmental fieldwork Why Work With Us? Contribute to protecting Tennessee's water quality and natural environment Join a friendly, diverse, and collaborative state team Real-world experience with potential career growth or full-time hire Mileage reimbursement and flexibility for remote work over time Make a difference in your community every single day

We are seeking a highly skilled Senior Scientist to oversee all aspects of Good Manufacturing Practices (GMP) and production within our Clinical Manufacturing Facility (CMF). This role involves close collaboration with the Manager and Supervisor of GMP Operations to provide hands-on support and leadership for daily GMP production activities, including project timeline management and personnel oversight. The Senior Scientist will play a crucial role in ensuring timely, compliant, and cost-effective production by leading staff and providing hands-on training to ensure adherence to best practices, batch records, and Standard Operating Procedures (SOPs). Responsibilities: * Solve, correct, and prevent problems as assigned by leadership, and delegate tasks to junior staff. * Work towards specific measurable objectives requiring operational planning skills with minimal direct supervision. * Lead and support a diverse and collaborative team environment, utilizing clear and concise communication to achieve high productivity and team success. * Provide leadership in daily operational activities related to GMP manufacturing of biological products, including leading and executing production processes, ensuring material availability, and maintaining proper documentation. * Set and maintain professional standards within the GMP area. * Collaborate with GMP Management to implement the strategic direction of the GMP area. * Support GMP resources and the supply chain, including ordering and maintaining materials inventory to meet production goals. * Maintain high standards of accurate documentation for all GMP operations. * Train and supervise junior staff to ensure proper operation of facility equipment and adherence to accurate documentation related to GMP activities and product quality. * Guide Operations Staff in deviation investigations, out-of-specification (OOS) results, and process troubleshooting in collaboration with GMP management and Quality Assurance. * Ensure continuous improvement objectives are identified and met using metrics and other statistical methods. Essential Skills: * Relevant four-year Life Science degree or Master's degree. * Five years of relevant experience with a four-year degree or two years with a Master's degree. * Background in the life sciences, biotechnology, or gene therapy industries. * Experience in a GMP or GLP setting. * Excellent communication, organization, and project management skills. * Proficiency in Microsoft Office (PowerPoint, Excel, Word), including data interpretation and reporting. * Technical writing/SOP writing experience. * Ability to work independently and collaboratively in a diverse and inclusive work environment. Additional Skills & Qualifications: * Knowledge of GMP or bioprocessing. * Experience in suspension or bioreactors. * Experience with downstream processing, tangential flow filtration (TFF), clarification, or large-scale cell culture. Pay and Benefits The pay range for this position is $31.00 - $36.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Columbus,OH. Application Deadline This position is anticipated to close on Apr 25, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: * Hiring diverse talent * Maintaining an inclusive environment through persistent self-reflection * Building a culture of care, engagement, and recognition with clear outcomes * Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Why Sarepta? Why Now? The promise of genetic medicine has arrived, and Sarepta is at the forefront. We hold leadership positions in Duchenne muscular dystrophy (DMD) and limb-girdle muscular dystrophies (LGMDs), and we currently have more than 40 programs in various stages of development in gene therapy, RNA and gene editing. In 2023, we launched our fourth therapy and the first ever gene therapy to treat Duchenne. We're looking for people who see unlimited potential in themselves and who are motivated by an unwavering commitment to patients. What Sarepta Offers At Sarepta, we care deeply about all the people in our community and believe in the importance of supporting them in all aspects of their lives. We aspire to maintain a culture that acknowledges people bring their whole selves to work, and we will strive to help everyone in our community integrate their work and personal lives while maintaining productivity. We are committed to offering a range of benefits and work-life resources designed to support people in the following areas: * Physical and Emotional Wellness * Financial Wellness * Support for Caregivers For a full list of our comprehensive benefits, see our website: ******************************* The Importance of the Role Nonclinical strategy and report management (NSRM) is a cross-functional group supporting nonclinical regulatory submissions and preparation of nonclinical documents. NSRM works with nonclinical research, nonclinical safety, immunology, regulatory, QC/QA and research operations groups to produce scientifically accurate and compliant documents including but not limited to SOPs, manuscripts, protocols, study reports, investigator brochures, IND and BLA modules. The nonclinical strategy and report management Scientist will primarily support the progression of a nonclinical program from research phase to development. This involves aiding in the compilation of nonclinical reports for an Investigational New Drug (IND) application. The nonclinical strategy and report management Scientist will be responsible for nonclinical data quality in reports submitted for regulatory filings, literature searches and reference checks, and drafting of study reports. The scientist will also be responsible for assisting in data interpretation and figure generation for reporting and may assist in statistical analysis of final data sets. Additional responsibilities include storyboard preparation and risk mitigation through collaborative problem solving. The position may shadow and potentially assist with in-lab activities on a limited basis to effectively perform their role. In collaboration with reporting leads, the nonclinical strategy and report management Scientist will be responsible for the management of study reports that will be used for internal purposes as well as for regulatory submissions. The Opportunity to Make a Difference * Aids in preparation of complex nonclinical and regulatory documents to support IND submissions including, but not limited to, protocols, study reports, amendments, investigator brochures, eCTD formatting, eCTD table and figure formatting, and IND/IMPD sections. * Reviews experimental results and interpretation of nonclinical data * Scientific contributor and subject matter expert who interprets data and applies knowledge of regulatory and scientific requirements to support document preparation * Effectively collaborates with cross-functional teams to produce clearly written, high-quality, and scientifically accurate documents and ensure consistency between related documents * High competency in writing, editing, and reviewing nonclinical and regulatory documents per company and other guidelines * Ensures accuracy of data reported in documents being filed with regulatory agencies * Performs and/or assists with quality control peer reviews of nonclinical documents * Identifies opportunities to improve operational efficiency and compliance and assesses regulatory guidelines for impact to nonclinical studies. * Demonstrated critical thinking and creative problem-solving skills across a range of scientific disciplines, including a constant grounding in analyses More about You * PhD with experience in cellular or molecular biology or related discipline * Excellent writing, presentation, and project management skills * Meticulous attention to detail and ability to comply with company style guides and templates * Ability to create strong, collaborative working relationships, operating as part of a team * Proficient in Graphpad Prism, RStudio/Python, Microsoft Excel, and Microsoft Word * Competent applying common statistical tests for data analysis * Excited to implement knowledge of FDA/international regulations, ICH guidelines, and applicable regulatory processes related to document preparation and production What Now? We're always looking for solution-oriented, critical thinkers. So, if you're comfortable with ambiguity and candor, relish challenging yourself, and place kindness and integrity at the forefront of how you approach your peers and work, then we encourage you to apply. #LI-Onsite Blank This position requires work on site at one of Sarepta's facilities in the United States. The targeted salary range for this position is $102,800 - $128,500 per year. Sarepta is making a good faith effort to be transparent and accurate around our hiring ranges. The salary offer is commensurate with Sarepta's compensation philosophy and considers factors including, but not limited to, education, training, experience, external market conditions, criticality of role, and internal equity. Candidates must be authorized to work in the U.S. Sarepta Therapeutics offers a competitive compensation and benefit package. Sarepta Therapeutics is an Equal Opportunity/Affirmative Action employer and participates in e-Verify.