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Clinical Research Regulatory Project Manager Jobs

UAB

CLINICAL RESEARCH REGULATORY COORDINATOR II

Tampa, FL · On-site

$47K - $77K/yr

The University of Alabama at Birmingham (UAB), O'Neal Comprehensive Cancer Center, is seeking a Clinical Research Regulatory Coordinator II. The O'Neal Comprehensive Cancer Center is one of 51 NCI ...

Innovo Research Inc

$22.75 - $30.50/hr

... managing clinical research data and documents, both regulatory and patient records. The CRC ... Performs other duties and projects as assigned.QUALIFICATIONSBachelor's degree in a related field1 ...

IQVIA

RWE Clinical Project Manager (FSP)

Durham, NC · On-site

$93K - $232K/yr

In this role, the clinical project manager will be responsible for end-to-end project delivery of ... clinical research regulatory requirements * Experience with primary and secondary data study ...

IQVIA, Inc.

RWE Clinical Project Manager (FSP)

Durham, NC · On-site

$93K - $232K/yr

In this role, the clinical project manager will be responsible for end-to-end project delivery of ... clinical research regulatory requirements * Experience with primary and secondary data study ...

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Clinical Research Regulatory Project Manager information

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How much do clinical research regulatory project manager jobs pay per year?

As of Sep 12, 2026, the average yearly pay for clinical research regulatory project manager in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

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Infographic showing various Clinical Research Regulatory Project Manager job openings in the United States as of September 2026, with employment types broken down into 85% Full Time, 11% Part Time, and 4% Contract. Highlights an 91% In-person, 2% Hybrid, and 7% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

CLINICAL RESEARCH REGULATORY COORDINATOR II (2)

Birmingham, AL • On-site

UAB NOVA RENT
See more jobs at UAB NOVA RENTexternal

$47K - $77K/yr

Full-time

Re-posted 6 days ago

Key responsibilities

  • Prepare, submit, and assist with research documentation including IRB submissions, consent forms, protocols, and safety reports.

  • Maintain regulatory documentation such as ICF, protocol, 1572, CVs, ML, IB, recruitment materials, and submission forms.

  • Prepare and maintain FDA applications for Investigational New Drugs (INDs) and Investigational Device Exemptions (IDEs).

Job description

The University of Alabama at Birmingham (UAB), O'Neal Comprehensive Cancer Center, is seeking a Clinical Research Regulatory Coordinator II.
The Clinical Research Regulatory Coordinator II will prepare, submit, and assist with multiple levels of research documentation, IRB submissions to UAB, WIRB, Advarra, and others. Maintain regulatory documentation, including ICF, protocol, 1572, CVs, ML, IB, recruitment materials, submission forms, and draft informed consents. Maintain/prepare FDA applications for Investigational New Drugs (INDs) and Investigational Device Exemptions (IDEs). To serve as a resource person or act as a consultant within the area of regulatory expertise.
The O'Neal Comprehensive Cancer Center is one of 51 NCI-designated comprehensive cancer centers in the United States and is the only one in Alabama and in the Deep South region. A comprehensive designation also means UAB Medicine patients have access to leading-edge treatments or clinical trials that they may not otherwise have at local community hospitals or smaller cancer centers. For many, an NCI designation can hold the key to survival. On campus and around Birmingham, the O'Neal Cancer Center is a significant part of our economic powerhouse. The O'Neal Cancer Center powers more than 400 scientists and physician-scientists, cares for 20,000 patients annually, and is home to more than 160 employees, plus all the physicians and clinical staff engaged in cancer patient care. The link to our website is: https://www.uab.edu/onealcancercenter/
Please attach a current resume with this application.
General Responsibilities
  • To prepare, submit, and assist with multiple levels of research documentation (i.e., IRB submissions, educational materials, reports, grant renewal reports, and study forms).
  • To maintain regulatory documentation, including consent forms, protocols, 1572s, CVs, licenses, investigator brochures, recruitment materials, safety reports, and submission forms.
  • To draft informed consents.
  • To prepare and maintain FDA applications for Investigational New Drugs (INDs) and Investigational Device Exemptions (IDEs).
  • To assist in drafting compliant advertisements.
  • To serve as resource person or act as consultant within area of regulatory expertise.
  • Performs other duties as assigned.

Annual Salary Range : $47,665 - $77,455
Qualifications
Bachelor's degree in a related field and three (3) years of related experience required. Work experience may substitute for education requirement.
Preferences
  • Advanced knowledge in regulatory matters related to clinical trials and retrospective IRBs.
  • Basic knowledge of clinicaltrials.gov, consenting, protocol review, adverse and serious adverse event reporting.
  • Ability to work independently, to make decisions, to interact with sponsors, regulatory authorities, and investigators.
  • Ability to communicate effectively with physicians, sponsors, and other collaborators.

UAB is an Equal Employment/Equal Educational Opportunity Institution dedicated to providing equal opportunities and equal access to all individuals regardless of race, color, religion, ethnic or national origin, sex (including pregnancy), genetic information, age, disability, and veteran's status. As required by Title IX, UAB prohibits sex discrimination in any education program or activity that it operates. Individuals may report concerns or questions to UAB's Assistant Vice President and Senior Title IX Coordinator. The Title IX notice of nondiscrimination is located at uab.edu/titleix.

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