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$40.5K

$95.4K

$138.5K

How much do research regulatory jobs pay per year?

As of Jul 27, 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 the highest paying job in regulatory affairs?

The highest paying roles in regulatory affairs are typically senior executive positions such as Director of Regulatory Affairs, Vice President, or Chief Regulatory Officer, which can earn six-figure salaries. These roles require extensive experience, advanced certifications, and leadership skills in managing compliance and regulatory strategies across organizations.

What are some common challenges faced by someone in a Research Regulatory role, 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 are Research Regulatory professionals?

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.

Is CRC entry level?

A Clinical Research Coordinator (CRC) position is often considered entry-level, especially for those with a bachelor's degree in a related field. However, some employers may prefer candidates with prior experience or certifications such as the Certified Clinical Research Professional (CCRP). Skills in data management, regulatory compliance, and communication are important for this role.

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.

Is a CRC higher than a CRA?

A Clinical Research Coordinator (CRC) and a Clinical Research Associate (CRA) are different roles in clinical trials; typically, a CRA has more responsibility and often a higher level of experience or seniority. CRAs usually oversee multiple sites, monitor trial progress, and ensure compliance, while CRCs handle day-to-day trial activities at a specific site. The hierarchy depends on the organization, but generally, CRAs are considered more senior than CRCs.

What is a research regulatory specialist?

A research regulatory specialist is a professional responsible for ensuring that clinical trials and research studies comply with government regulations and institutional policies. They prepare and review documentation, coordinate with regulatory agencies, and monitor study progress to maintain compliance and facilitate approval processes.

What are the key skills and qualifications needed to thrive as a Research Regulatory professional, and why are they important?

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.
More about Research Regulatory jobs
What cities are hiring for Research Regulatory jobs? Cities with the most Research Regulatory job openings:
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Research Regulatory jobs near you
Infographic showing various Research Regulatory job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 86% Full Time, 10% Part Time, and 3% Contract. Highlights an 91% Physical, 4% Hybrid, and 5% Remote job distribution, with an average salary of $95,411 per year, or $45.9 per hour.
Research Regulatory Specialist

Research Regulatory Specialist

BayCare Health System

Clearwater, FL • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 19 days ago

BayCare Health System rating

7.5

Company rating: 7.5 out of 10

Based on 398 frontline employees who took The Breakroom Quiz

230th of 890 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: Research Regulatory Specialist
Facility: BayCare Systems Office (Hybrid)
Schedule: Tuesday - Thursday in office; Monday and Friday work from home
Responsibilities:
  • Responsible for ensuring their assigned research team members, investigators and associated portfolio of clinical research projects are in compliance with all applicable institutional, sponsor and governmental policies and laws.
  • Acts as a liaison between the sponsor, Clinical Research Operations, Institutional Review Board and internal departments/ staff to complete initial Institutional Review Board protocol submissions.
  • Submit study amendments in a timely fashion including changes to the protocol, consent forms and other study documents.
  • Prepare for and facilitate monitoring visits, ensure study regulatory files are up to date & audit ready
  • Maintain regulatory master files for industry & investigator initiated clinical trials
  • Aid in the development of protocol specific standard operation procedures, and develop & train Clinical Research Coordinators on guidelines related to consent, ethical conduct and protection of human subjects.
  • Must have extensive knowledge of FDA regulation and human subjects protection

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 & Education Requirements:
  • Required - Master's Degree in Related Field with 1 Year of Research, Regulatory, or other Healthcare Administration experience
  • Or - Bachelor's Degree in Business, Healthcare Management, Nursing or Related Field and 2 Years of Research Regulatory or other Healthcare Administration experience
  • Or - High School Diploma with 5 Years of Research Regulatory Experience

Certification
  • 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: No
Shift Hours: 7:00AM - 3:30PM; 8:00AM - 4:30PM
Weekend Work: None
Equal Opportunity Employer Veterans/Disabled

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