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Research Regulatory Jobs (NOW HIRING)

ThedaCare

Research Regulatory Coordinator

Neenah, WI · On-site

The Research Regulatory Coordinator manages compliance, documentation, and submissions for clinical trials and human subject's research. This role acts as the primary liaison between clinical ...

Carle Health

Research Regulatory Coordinator

Urbana, IL · On-site

$24.50 - $32.50/hr

Overview The Clinical Research Regulatory Coordinator is a specialized research professional that facilitates and coordinates the regulatory aspects of a clinical trial and plays a critical role in ...

Carle Health

Research Regulatory Coordinator

Urbana, IL · On-site

$25.81 - $43.10/hr

Overview The Clinical Research Regulatory Coordinator is a specialized research professional that facilitates and coordinates the regulatory aspects of a clinical trial and plays a critical role in ...

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Research Regulatory information

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$40.5K

$95.4K

$138.5K

How much do research regulatory jobs pay per year?

As of Aug 21, 2026, the average yearly pay for research regulatory in the United States is $95,411.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,500.00 and $112,000.00 per year, depending on experience, location, and employer.

What is a research regulatory professional?

Research Regulatory professionals are individuals who ensure that research studies, particularly those involving human subjects, comply with federal, state, and institutional regulations. They review study protocols, prepare and submit necessary documents to Institutional Review Boards (IRBs), and monitor ongoing research for continued compliance. Their work helps protect the rights and welfare of research participants while supporting researchers in meeting all legal and ethical requirements.

What skills and qualifications are needed to thrive as a research regulatory professional?

To thrive as a Research Regulatory professional, you need a solid understanding of clinical research processes, regulatory compliance, and ethical guidelines, often supported by a degree in life sciences or healthcare and relevant experience. Familiarity with regulatory submission systems, IRB processes, and certifications such as CCRA or CCRC is highly beneficial. Strong attention to detail, organizational skills, and effective communication are crucial soft skills for managing complex documentation and liaising with stakeholders. These skills ensure research studies comply with legal and ethical standards, safeguarding both data integrity and participant safety.

What are common challenges faced by research regulatory professionals, and how can they be addressed?

Professionals in Research Regulatory roles often encounter challenges such as keeping up-to-date with frequently changing regulations, ensuring all study documentation is accurate and complete, and managing communication between research teams and regulatory bodies. Addressing these challenges requires strong organizational skills, continual education on regulatory updates, and a proactive approach to collaborating with both internal and external stakeholders. Developing robust tracking systems and maintaining clear documentation can also help streamline processes and reduce compliance risks.

What is the difference between Research Regulatory vs Research Compliance Officer?

AspectResearch RegulatoryResearch Compliance Officer
CredentialsTypically requires degrees in life sciences, regulatory affairs certificationsOften holds degrees in related fields, compliance certifications
Work EnvironmentResearch labs, regulatory agencies, pharmaceutical companiesResearch institutions, healthcare organizations, biotech firms
Employer & IndustryPharmaceutical, biotech, academic researchResearch institutions, hospitals, biotech companies

Research Regulatory professionals focus on ensuring research activities comply with regulations and obtain necessary approvals. Research Compliance Officers oversee adherence to policies and standards within research settings. While both roles ensure regulatory adherence, Research Regulatory specialists primarily handle regulatory submissions and approvals, whereas Research Compliance Officers monitor ongoing compliance and policy implementation.

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Research Regulatory jobs near you
Infographic showing various Research Regulatory job openings in the United States as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 85% Full Time, 11% Part Time, and 2% Contract. Highlights an 84% Physical, 4% Hybrid, and 12% Remote job distribution, with an average salary of $95,411 per year, or $45.9 per hour.

Supervisor Research Regulatory

BayCare Health System

Clearwater, FL • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 14 days ago

BayCare Health System rating

7.5

Company rating: 7.5 out of 10

Based on 403 frontline employees who took The Breakroom Quiz

237th of 891 rated healthcare providers

Job description

Join the team that is revolutionizing health care - BayCare Health System
Our network consists of 16 community-based hospitals, a long-term acute care facility, home health services, outpatient centers and thousands of physicians. With the support of more than 30,000 team members, we promote a forward-thinking philosophy that's built on a foundation of trust, dignity, respect, responsibility, and clinical excellence.
Title: Supervisor Research Regulatory
Facility: BayCare System Office (Hybrid)
Responsibilities Include:
  • Responsible for supervising a regulatory specialist team, ensuring compliance with regulations, managing regulations submissions to Local and Central IRBs, and overseeing the preparation of necessary documentation for clinical trials.
  • This role requires strong teamwork, communication, regulatory knowledge and skills to guide the team to ensure research protocols are conducted in compliance with all regulations.
  • The supervisor directly coordinates regulatory oversight for human subject's research projects administratively approved for use within BayCare, registers BayCare-sponsored projects on ClinicalTrials.gov, and prepares and submits IND or IDE applications to the FDA for BayCare-sponsored projects as required.
  • Required skills includes extensive knowledge of FDA regulations and human subject protection, regulatory knowledge and compliance, leadership and team management, operational oversight, communication and collaboration and analytical and problem-solving skills.

BayCare offers a competitive total reward package including:
  • Benefits (Medical, Dental, Vision)
  • Paid Time Off
  • Tuition Assistance
  • 401K Match and additional yearly contribution
  • Annual performance appraisals and team award bonus
  • Family resources and wellness opportunities
  • Community perks and discounts

Experience Requirements
  • Required - 3 years research regulatory submissions experience

Education Requirements
  • Required - Bachelor's Degree in Business or Healthcare Management

Certification Requirements
  • Preferred - SOCRA (Society of Clinical Research Associates)
  • Preferred - ACRP (Association of Clinical Research Professionals)
  • Preferred - CCRC (Certified Clinical Research Coordinator)

Location: Clearwater, FL
Status: Full Time; Exempt
Shift Hours: 8:00AM - 4:30PM
Weekend Work: None
Equal Opportunity Employer Veterans/Disabled

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