Pediatric Clinical Research Manager, HIV & ID

University of Florida College of Medicine - Jacksonville

Jacksonville (FL)

On-site

USD 82,000 - 85,000

Full time

11 hours ago
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Job summary

University of Florida College of Medicine - Jacksonville is seeking a Manager, Clinical Research - Peds ID to oversee the UF CARES clinical research program. You will lead operational activities, supervise coordinators, and ensure regulatory compliance across HIV-related and non-HIV studies.

The role focuses on study start-up, ongoing operations, and closeout while coordinating with investigators, sponsors, and regulatory bodies to optimize research performance.

Qualifications

  • Masters degree in appropriate area of specialization; or a bachelors degree and two years of experience.
  • Obtain and maintain Shipping Dangerous goods certification and obtain and maintain CITI and NIH Certification within 3 months to maintain employment.
  • Working knowledge of computers and computer software such as MS Word, Excel, and Outlook

Responsibilities

  • Oversees management and coordination of clinical research activities within UF CARES.
  • Provides operational leadership for HIV-related and non-HIV research protocols.
  • Supervises Clinical Research Coordinators and assigns workload, training, and performance.
  • Directs study start-up, implementation, ongoing operations, and closeout processes.
  • Ensures regulatory compliance and quality assurance across the program.
  • Manages budgets, sponsor billing, and financial activity for studies.
  • Coordinates with PI, sponsors, regulatory bodies, and university offices to ensure compliance.

Education

Master's degree in appropriate area
Bachelor's degree with 2 years experience

Tools

MS Word
Excel
Outlook

Job description

University of Florida College of Medicine - Jacksonville is seeking a Manager, Clinical Research - Peds ID to oversee the UF CARES clinical research program. You will lead operational activities, supervise coordinators, and ensure regulatory compliance across HIV-related and non-HIV studies.

The role focuses on study start-up, ongoing operations, and closeout while coordinating with investigators, sponsors, and regulatory bodies to optimize research performance.

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