How is Clinical Trials used?
Zippia reviewed thousands of resumes to understand how clinical trials is used in different jobs. Explore the list of common job responsibilities related to clinical trials below:
- Provide and discuss information relating to key scientific investigations and clinical trials
- Processed and maintained adverse event reports and clinical trial data.
- submit study summaries to IRB, register clinical trials with clinicaltrials.gov and initiate cross-functional team meetings/teleconferences and meeting summaries).
- Supervised clinical trial development program identified regulatory risks/benefits, monitored site and study compliance and managed developmental strategies for trials.
- Reviewed and assessed serious spontaneous reports of adverse events and performed causality assessment of clinical trials and solicited reports.
- Participate in the development and implementation of new clinical molecular diagnostic testing procedures and clinical trial tests.
Are Clinical Trials skills in demand?
Yes, clinical trials skills are in demand today. Currently, 15,390 job openings list clinical trials skills as a requirement. The job descriptions that most frequently include clinical trials skills are medical scientist, principal biostatistician, and associate director of biostatistics.
How hard is it to learn Clinical Trials?
Based on the average complexity level of the jobs that use clinical trials the most: medical scientist, principal biostatistician, and associate director of biostatistics. The complexity level of these jobs is advanced.
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What jobs can you get with Clinical Trials skills?
You can get a job as a medical scientist, principal biostatistician, and associate director of biostatistics with clinical trials skills. After analyzing resumes and job postings, we identified these as the most common job titles for candidates with clinical trials skills.
Medical Scientist
Job description:
Medical scientists are medical professionals who conduct research by using clinical trials and other investigative methods to reach findings that will improve overall human health. These scientists must design and conduct studies that investigate human diseases while discovering methods to prevent and treat them. They must standardize the potency and doses of drugs so that they can mass-produce and distribute them and medicinal compounds to the public. Medical scientists must also partner with health departments, industry personnel, and physicians to develop programs that improve health outcomes.
- Clinical Trials
- Regulatory Submissions
- Advisory Boards
- Risk Management
- External Stakeholders
- Medical Writing
Principal Biostatistician
Job description:
Principal biostatisticians are professionals who are responsible for communicating all the activities related to biostatistics of assigned projects to the sponsor companies. These biostatisticians are required to participate in the development of finished products used in clinical trials and provide statistical oversight to ensure data integrity and appropriate analysis are performed. They must develop customized statistical programs that can generate statistical data listings, summary tables, and figures. Principal biostatisticians must also answer all the questions from regulatory authorities appropriately.
- Clinical Trials
- QC
- Statistical Analysis
- Clinical Study Reports
- Statistical Methods
- Statistical Reports
Associate Director Of Biostatistics
- SAS
- Clinical Trials
- FDA
- Statistical Support
- Study Design
- CRO
Clinical Trial Coordinator
Job description:
A clinical trial coordinator is responsible for assisting in medical trials and clinical research studies. Clinical trial coordinators support the whole operational process of medical research from its conceptualization until the final outputs. They manage the adequacy of tools and equipment, ensuring the cleanliness and orderliness of the facilities to prevent potential hazards and delays in laboratory testing. A clinical trial coordinator must have excellent communication and organizational skills, especially in writing progress reports and securing the acquired laboratory samples.
- Clinical Trials
- Patients
- Informed Consent
- IRB
- Meeting Minutes
- FDA
Clinical Research Director
Job description:
Clinical research directors are responsible for providing leadership in a clinical research setting. These directors oversee the development and evaluation of drugs and the program designs to prevent and treat contagious diseases as a part of their main responsibility. They gather information on progress reports and create new strategies to present them to higher management. This job requires them to have strong communication and leadership skills to thrive in their role and confidence in themselves to perform their duties without worry.
- Patients
- Clinical Trials
- Oversight
- FDA
- GCP
- Clinical Development
Clinical Research Monitor
Job description:
A clinical research monitor monitors all data, observations, information, and feedback from research and experiments. A clinical research monitor is essential in any research laboratory as accurate measurements and collation of data is essential for proper determination and interpretation. In the medical field of study, data accuracy is an absolute necessity as the prescribing of proper medication is only possible if the diagnosis is precise, based on accurate data results of tests. Other additional tasks of a clinical research monitor are organizing data, providing reports, and suggesting improvements in data gathering and monitoring.
- FDA
- Clinical Trials
- Informed Consent
- IRB
- ICH-GCP
- Clinical Operations
Clinical Trials Specialist
Job description:
A Clinical Trials specialist assist in the daily activities involved in clinical trials. This includes gathering facts, information, and observed data and helps analyze and interpret results. Clinic trials are essential in developing new medicines and vaccines needed for the safeguard of human health. Alongside this primary responsibility, it is also the clinical trial specialist's task to organize data, monitor laboratory equipment, and ensure all specimens needed for the trials are according to instructions.
- Patients
- Clinical Research
- Clinical Trials
- Informed Consent
- FDA
- Consent Forms
Senior Site Manager
Job description:
A senior site manager oversees construction sites to ensure projects are completed on time. They create budgets, coordinate with clients, and supervise workers. They must also maintain quality control procedures and minimize risks.
- Informed Consent
- Clinical Trial Management
- Clinical Trials
- FDA
- IRB
- QA
Cancer Researcher
Job description:
A cancer researcher is a medical scientist who devotes their time working at laboratories to study and discover ways to diagnose and treat cancer, saving countless people's lives in the process. Their duties usually include gathering and analyzing samples through basic or complex laboratory processes, studying existing cases from people of all ages, organizing specimens and instruments, coordinating with fellow experts, conducting experiments, and maintaining extensive records. Moreover, as a cancer researcher, it is essential to keep an open communication line with fellow researchers, collaborating efforts for a smooth workflow.
- Patients
- Clinical Research
- Clinical Trials
- Data Collection
- Patient Care
- Informed Consent
Clinical Researcher
Job description:
A clinical researcher is primarily in charge of conducting research trials for medicine and health care development. Their responsibilities mainly revolve around conducting extensive research and analysis by gathering samples, performing experiments, working with research participants, and collaborating with other researchers and scientists. Moreover, as a clinical researcher, it is essential to maintain records of all experiments, summarize findings into reports and presentations, and monitor every progress, all while adhering to the research's deadlines, budgets, goals, and policies.
- Patients
- Informed Consent
- IRB
- Clinical Trials
- Data Collection
- FDA
Clinical Research Specialist
Job description:
An air traffic controller specializes in overseeing and directing airspace traffic, all while maintaining an active line of communication with aircraft to ensure safe and efficient air travels. Generally assigned in ground control centers and towers, an air traffic controller's responsibilities revolve around utilizing technology to monitor flight paths, weather, and airport runways to guide pilots and airport personnel. They also work on coordinating with other control officers, inspecting and maintaining instruments and equipment in good condition, and alerting departments and assigned personnel should there be any emergencies.
- Patients
- Clinical Trials
- Informed Consent
- Data Collection
- IRB
- Research Data
Operations Research Manager
Job description:
An operations research analysis manager is a key leader in an organization who oversees the collection and analysis of operations data, analyzes the information for deficiencies, and makes recommendations to improve. With a team of operations research analysts, the operations research analysis manager identifies inefficiencies in an operation and offers solutions to eliminate the inefficiencies detected. Operations research analysis managers provide leadership and strategy in the operations research department to help realize better efficiency.
- Research Operations
- Research Projects
- Project Management
- Clinical Trials
- Oversight
- Data Collection
Clinical Research Scientist
Job description:
A clinical research scientist is responsible for assisting physicians in conducting laboratory research and examinations to identify diseases and establish treatment plans. They also inspect medical tools and equipment to prevent hazards and operational delays. A clinical research scientist must have excellent communication skills and extensive knowledge of the medical industry to provide the highest quality care services for the patients.
- Clinical Research
- Clinical Trials
- Clinical Development
- Data Management
- Oncology
- Clinical Data
Senior Clinical Research Scientist
Job description:
A senior clinical research scientist has to identify various diseases among their patients and conduct clinical investigations. Once they identify a disease and its cause, they assist physicians in the treatment of patients. They also have to analyze clinical data and health tests. They should have the ability to develop new research methods.
- Clinical Operations
- Informed Consent
- Clinical Development
- Clinical Trials
- Clinical Data
- Consent Forms
Senior Statistician
Job description:
A senior statistician specializes in gathering and interpreting data through mathematical techniques, drawing conclusions that will play a significant role in a company's decision-making procedures. Their responsibilities typically include liaising with different departments to collect data, maintaining databases, performing various tests and assessments, keeping an eye on any errors or discrepancies, and presenting findings using graphs, charts, and reports. Moreover, as a senior statistician, it is essential to lead and oversee the performance of junior statisticians, all while promoting and enforcing the company's policies and regulations.
- Statistical Methods
- Data Analysis
- Healthcare
- Data Management
- Clinical Trials
- Study Design
Clinical Research Associate
Job description:
A clinical research associate is responsible for assisting medical professionals in clinical trials and conducting research studies on medications and medical procedures. Clinical research associates monitor the research materials, ensuring its safety and reliability through trial procedures, writing comprehensive reports of results, and disseminating information across the concerned parties. They also provide recommendations on improving clinical processes, reiterating protocol requirements, and maintaining strict confidentiality of the trial subjects. A clinical research associate must have extensive knowledge of the medical industry, including its disciplines and principles, to perform duties accurately under minimal supervision.
- Patients
- Informed Consent
- CRA
- Clinical Trials
- Clinical Trial Management
- Oncology
Clinical Project Manager
Job description:
A clinical project manager specializes in developing and organizing clinical trials. Their responsibilities revolve around planning and coordinating with all necessary personnel and experts, scheduling meetings, and preparing necessary documentation, ensuring compliance with all laws and regulations. Moreover, a clinical project manager must devise strategies and train all staff, develop protocols and guidelines, coordinate with vendors and suppliers, evaluate staff and verify documentation, and assist in all activities to ensure that every process aligns with the project's agenda. Should there be any issues or concerns, a clinical project manager must conduct corrective measures right away.
- Manage Cross
- Patients
- Clinical Research
- Project Management
- Clinical Trials
- Oversight
Quality Assurance Auditor
Job description:
Quality assurance (QA) analysts are responsible for testing company products and processes. Through testing, QA analysts ensure that the product or process is ready for production. They check whether the process meets company standards and guidelines, as well as any standards related to the industry they are in. QA analysts are in charge of determining the root cause of any problems that they may encounter. They also try to solve these as soon as possible. They also ensure that the company's products meet user expectations as well as the company's brand promise.
- Patients
- ISO
- Clinical Trials
- FDA
- Quality Assurance Audits
- GMP
Cancer Center Director
Job description:
Cancer Center Directors provide direction and strategic leadership for the cancer center. The directors lead daily operations in the organization such as planning, organizing, resource management, and staffing. They take part in the recruitment and evaluation processes for clinic or hospital positions. Part of their job is to coordinate programs for the cancer center. Among their other responsibilities are the creation of new treatment program methods, a delegation of responsibilities, and set-up goals for the clinic's departments.
- Patients
- Oncology
- Patient Care
- Clinical Trials
- Customer Service
- Chemotherapy
How much can you earn with Clinical Trials skills?
You can earn up to $88,852 a year with clinical trials skills if you become a medical scientist, the highest-paying job that requires clinical trials skills. Principal biostatisticians can earn the second-highest salary among jobs that use Python, $120,026 a year.
Job Title![]() ![]() | Average Salary![]() ![]() | Hourly Rate![]() ![]() |
---|---|---|
Medical Scientist | $88,852 | $43 |
Principal Biostatistician | $120,026 | $58 |
Associate Director Of Biostatistics | $140,422 | $68 |
Clinical Trial Coordinator | $50,720 | $24 |
Clinical Research Director | $100,744 | $48 |
Companies using Clinical Trials in 2025
The top companies that look for employees with clinical trials skills are Johnson & Johnson, Merck, and Sanofi US. In the millions of job postings we reviewed, these companies mention clinical trials skills most frequently.
Rank![]() ![]() | Company![]() ![]() | % Of All Skills![]() ![]() | Job Openings![]() ![]() |
---|---|---|---|
1 | Johnson & Johnson | 15% | 930 |
2 | Merck | 14% | 1,446 |
3 | Sanofi US | 9% | 1,217 |
4 | Takeda Pharmaceuticals U.S.A., Inc. | 9% | 1,031 |
5 | Bristol-Myers Squibb | 9% | 604 |
Departments using Clinical Trials
Department![]() ![]() | Average Salary![]() ![]() |
---|---|
Healthcare | $83,931 |
Research & Development | $71,003 |
6 courses for Clinical Trials skills
1. Clinical Trials Operations
This specialization is designed for individuals and teams that will be running or interacting with clinical trials. In four courses, learners will develop insights and build the skills they need to design, manage, and monitor clinical trials as well as analyze, document, and communicate the results. Learners will also learn best practices regarding ethics, safety, participant recruitment, regulatory compliance, and reporting standards. The core principles and skills of the specialization will lay the foundation for a successful career in the field...
2. Clinical Trials Analysis, Monitoring, and Presentation
In this course, you’ll learn more advanced operational skills that you and your team need to run a successful clinical trial. You’ll learn about the computation of sample size and how to develop a sample size calculation that’s suitable for your trial design and outcome measures. You’ll also learn to use statistical methods to monitor your trial for safety, integrity, and efficacy. Next, you’ll learn how to report the results from your clinical trials through both journal articles and data monitoring reports. Finally, we’ll discuss the role of the analyst throughout the trial process, plus a few additional topics such as simulations and adaptive designs...
3. Design and Conduct of Clinical Trials
In this course, you’ll learn how to design and carry out clinical trials. Each design choice has implications for the quality and validity of your results. This course provides you and your team with essential skills to evaluate options, make good design choices, and implement them within your trial. You’ll learn to control for bias, randomize participants, mask treatments and outcomes, identify errors, develop and test hypotheses, and define appropriate outcomes. Finally, a trial without participants is no trial at all, so you’ll learn the guiding principles and develop the essential skills to ethically and conscientiously recruit, obtain consent from, and retain trial participants...
4. Clinical Trials Data Management and Quality Assurance
In this course, you’ll learn to collect and care for the data gathered during your trial and how to prevent mistakes and errors through quality assurance practices. Clinical trials generate an enormous amount of data, so you and your team must plan carefully by choosing the right collection instruments, systems, and measures to protect the integrity of your trial data. You’ll learn how to assemble, clean, and de-identify your datasets. Finally, you’ll learn to find and correct deficiencies through performance monitoring, manage treatment interventions, and implement quality assurance protocols...
5. Hack into SAS Clinical Trials Programming Certification
This course aims to largely shorten your time (and save money) for preparing the clinical programming certification exam when you possess SAS Base and some advanced programming techniques and experience. It includes the following: Introduction to the exam: an exhaustive list of exam contents, books, references and registration (pricing, length, no. of questions, format, etc.)A road map for SAS programmer to Clinical programming (with the focus of theory of clinical trial and industrial regulations and standards)Clinical programming with coding examples in SASA mock exam on the classic questionsI have been working in the pharmaceutical industry for many years. In my early days of job seeking, I was certified as a Clinical Trial Programmer Using SAS 9 and it really helped me. Getting the clinical programming certificate is the first and the most important step towards a clinical programmer. It will surely help you get a higher response rate for your job application. More importantly, it helps you understand many important concepts and the application of SAS programming skills in a clinical context that are often questioned during job interviews. I am sure you would enjoy this crash course with the aim of shortening your preparation time and boost the success rate. Let's hack into the clinical programming certification and be prepared for the certification exam!...
6. The Simplest Guide to Clinical Trials Data Analysis with SAS
This course gives an introduction to the Pharmaceutical/ Life Science industry in a simple and visual style that is easy to understand. It shows how SAS is used as a tool to work with the vast amount of clinical data within this industry. The course takes you through an example clinical study sample data, and generate various Clinical Study Reports that are submitted to the FDA (in the US) or other regulatory authorities in other countries. You will not only hone your SAS programming skills but will also learn essential concepts needed to work in the Pharma industry in the areas of Biostatistics and Clinical Data Management. After the introduction to the pharma industry and learning relevant concepts about Clinical Trials, the course takes you through a hands-on training exercise to build the very important and fundamental Clinical Study Report called the Demographics Table. You will begin with a sample clinical study data in an Excel sheet, then you will import it into SAS, derive all necessary variables as shown in the mock table, and finally generate a clinical study report. All this will be done using guided SAS Programming steps with detailed explanations at every step of programming. At the end of this course, you will have learnt to work with Clinical Study Data, generate a real Clinical Study Report, and extend those steps to build other reports that constitute Clinical Trial submissions to the regulatory bodies. Prerequisites: You will need basic SAS programming knowledge to work with code discussed in this course. You can take my course on SAS programming (The Simplest Guide to SAS Programming) available on Udemy. A guide to the following SAS certification exam: SAS Certified Clinical Trials Programmer Using SAS®9Earn a CertificateWhen you finish listening to all videos, assignments, quizzes and practice exams, you'll earn a Certificate that you can share with prospective employers and your professional network...