Research Program Manager II — Growth & IRB Compliance

University of Florida Jacksonville Physicians, Inc.

Jacksonville (FL)

On-site

USD 85,000 - 120,000

Full time

34 hours ago
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Job summary

University of Florida Jacksonville Physicians, Inc. seeks a Research Manager to plan and coordinate the Department’s research function and resources, including personnel, protocols, logistics, and clinical research practice.

Responsibilities include organizing research activities, maintaining regulatory documentation, ensuring IRB compliance, vendor study coordination, and staff training. Travel up to 10% is expected; a Bachelor's degree is required and a Master's is preferred.

Qualifications

  • 3–5 years management experience required.
  • 3–5 years progressive research experience required.
  • Bachelor's degree in Public Health Science, Management or related field required.
  • Master's degree preferred.
  • Travel up to 10%.

Responsibilities

  • Organize the research activities of the Department and establish Research Office for the Department to manage all Research operations.
  • Develop and maintain a system of organized and easily retrievable regulatory and organizational documentation for all studies.
  • Ensure research trials are conducted within UFHSC IRB and comply with all Federal, State, and Local regulations and guidelines with respectto research proceedings. Oversee all regulatory requirements of research projects.
  • Identify and Procure vendor studies. Coordinate proposal development, budgeting, submissions, approvals and closeout through IRB andstudy sponsors. Organize study start-up and regulatory document collection.
  • Evaluate, Develop and conduct training/education programs.
  • All other duties as assigned.

Skills

Management experience
Research experience

Education

Bachelor's degree
Master's degree

Job description

University of Florida Jacksonville Physicians, Inc. seeks a Research Manager to plan and coordinate the Department’s research function and resources, including personnel, protocols, logistics, and clinical research practice.

Responsibilities include organizing research activities, maintaining regulatory documentation, ensuring IRB compliance, vendor study coordination, and staff training. Travel up to 10% is expected; a Bachelor's degree is required and a Master's is preferred.

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