What is Regulatory Submissions?
Regulatory Submissions offers a readable and clearly written road map for effective submission of documents for required regulatory reviews during product development.
How is Regulatory Submissions used?
Zippia reviewed thousands of resumes to understand how regulatory submissions is used in different jobs. Explore the list of common job responsibilities related to regulatory submissions below:
- Developed comprehensive SAPs for both independent projects and integrated summaries of safety and efficacy for regulatory submissions.
- Format documents intended for regulatory submissions in accordance with company style manual to ensure they meet requirements for electronic submissions.
- Identify, obtain, compile and review regulatory documents for regulatory submissions, striving for quality submissions and expedited approvals.
- Provided Regulatory compliance support and review of regulatory submissions, approvals, product labeling, registrations and other projects.
- Familiarized with US health agency guidelines, granularity and modules pertaining to paper and electronic regulatory submissions.
- Managed emails for regulatory submissions and distribute all necessary summaries and reports to applicable recipient.
Are Regulatory Submissions skills in demand?
Yes, regulatory submissions skills are in demand today. Currently, 3,267 job openings list regulatory submissions skills as a requirement. The job descriptions that most frequently include regulatory submissions skills are biostatistics director, regulatory affairs associate, and medical scientist.
How hard is it to learn Regulatory Submissions?
Based on the average complexity level of the jobs that use regulatory submissions the most: biostatistics director, regulatory affairs associate, and medical scientist. The complexity level of these jobs is challenging.
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What jobs can you get with Regulatory Submissions skills?
You can get a job as a biostatistics director, regulatory affairs associate, and medical scientist with regulatory submissions skills. After analyzing resumes and job postings, we identified these as the most common job titles for candidates with regulatory submissions skills.
Biostatistics Director
- SAS
- CRO
- Regulatory Submissions
- Study Design
- Biometrics
- Statistical Analysis
Regulatory Affairs Associate
Job description:
A regulatory affairs associate is in charge of learning and implementing company policies and government regulations, ensuring compliance in every aspect of the company. Their responsibilities revolve around coordinating with different departments to gather data, conducting inspections and assessments, reviewing existing procedures, liaising with external agencies, and producing progress reports. They may also participate in instructing employees of the standards one must uphold. Furthermore, as a regulatory affairs associate, it is essential to develop guidelines and standards on every procedure in adherence to the latest policies and regulations.
- Regulatory Affairs
- FDA
- Regulatory Submissions
- Medical Devices
- Global Regulatory
- Regulatory Agencies
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
Scientific Writer
Job description:
Scientific writers are professionals who are responsible for conducting research and writing articles that are related to scientific topics for many different kinds of publications and scientific journals. These writers are required to conduct interviews with scientists and other important people to ensure accurate information about the essays they are writing. They must adapt and comply with in-house style guides as well as perform copy-editing and proofreading duties. Scientific writers must also build up a network of contacts with other professionals in the industry such as press officers, PR executives, and researchers.
- IND
- NDA
- Abstracts
- Regulatory Submissions
- Proofreading
- Clinical Study Reports
Senior Staff Scientist
Job description:
A Senior Staff Scientist is responsible for supervising projects and activities of a company. They manage the technical, budgetary, and scheduling aspects of scientific research projects.
- Data Analysis
- FDA
- Next-Generation Sequencing
- Statistical Analysis
- Regulatory Submissions
- PK
Regulatory Specialist
Job description:
A regulatory specialist is responsible for evaluating all the business processes, functions, and requirements and ensure its compliance with the company's protocols and state regulations. Regulatory specialists conduct regular audits, review the company's documents and business transactions, renew permits and licenses, and submit necessary files required by regulatory agencies. They coordinate with the management to revise the company's handbook accordingly and disseminate information on any changes across the organization. A regulatory specialist may also facilitate training programs and orientation to inform the employees on risk policies to avoid reputational issues, potential hazards, and delays in operations.
- FDA
- Regulatory Compliance
- Regulatory Agencies
- Regulatory Submissions
- Customer Service
- Clinical Trials
Regulatory Affairs Manager
Job description:
A regulatory affairs manager is in charge of ensuring that all aspects of a company adhere to the rules and regulations set by regulatory agencies. Their responsibilities revolve around devising regulation compliance strategies, creating training and orientation programs to inform the staff on the policies and standards, conducting internal inspections and information drives, and keeping abreast with the latest rules and regulations. Moreover, a regulatory affairs manager is in charge of processing and submitting necessary documents to government agencies, ensuring compliance and timeliness.
- Regulatory Affairs
- FDA
- Medical Devices
- Regulatory Submissions
- Regulatory Agencies
- Global Regulatory
Public Affairs Internship
Job description:
A public affairs intern is responsible for performing administrative duties to support the public affairs operations on media relations and developing strategies to maintain the department's integrity for social responsibility. Public affairs interns assist with press releases, community programs, and dissemination of information to the public. They also check the communication techniques, ensuring that the approach reaches the target audience, as well as responding to the public's inquiries and concerns and escalating complaints. A public affairs intern must have excellent communication and organizational skills, especially on data processing and publishing accurate content on different medium platforms.
- Public Affairs
- Press Releases
- PowerPoint
- Public Policy
- Regulatory Submissions
- Community Outreach
How much can you earn with Regulatory Submissions skills?
You can earn up to $58,329 a year with regulatory submissions skills if you become a biostatistics director, the highest-paying job that requires regulatory submissions skills. Regulatory affairs associates can earn the second-highest salary among jobs that use Python, $71,154 a year.
Job Title![]() ![]() | Average Salary![]() ![]() | Hourly Rate![]() ![]() |
---|---|---|
Biostatistics Director | $58,329 | $28 |
Regulatory Affairs Associate | $71,154 | $34 |
Medical Scientist | $88,852 | $43 |
Scientific Writer | $99,550 | $48 |
Senior Staff Scientist | $123,740 | $59 |
Companies using Regulatory Submissions in 2025
The top companies that look for employees with regulatory submissions skills are Johnson & Johnson, Bristol-Myers Squibb, and Takeda Pharmaceuticals U.S.A., Inc. In the millions of job postings we reviewed, these companies mention regulatory submissions skills most frequently.
Rank![]() ![]() | Company![]() ![]() | % Of All Skills![]() ![]() | Job Openings![]() ![]() |
---|---|---|---|
1 | Johnson & Johnson | 15% | 1,014 |
2 | Bristol-Myers Squibb | 13% | 544 |
3 | Takeda Pharmaceuticals U.S.A., Inc. | 10% | 1,163 |
4 | QuintilesIMS | 9% | 656 |
5 | Sumitomo Corporation | 9% | 246 |
Departments using Regulatory Submissions
Department![]() ![]() | Average Salary![]() ![]() |
---|---|
Marketing | $98,496 |
Research & Development | $81,255 |