Clinical Research Program Coordinator - Core-Ctr For Research Excel

Tampa General Hospital, Inc.; Tampa (FL); Remote; USD 65,000 - 90,000; Full time

Job summary

Tampa General Hospital is seeking a Clinical Research Program Coordinator to support the Core-Ctr For Research Excel. The role involves coordinating clinical studies, reviewing budgets and agreements, ensuring IRB approvals, and maintaining study documentation.

Applicants typically have a Bachelor’s degree in a related field and 3 years of experience in research administration or project management. The position is fully remote eligible and located at the TGH Main Campus in Tampa, FL.

Qualifications

• Bachelor's degree in a related field is required.
• 3 years experience in research administration, clinical research, or project management.

Responsibilities

• Coordinate clinical research studies and new sponsored projects.
• Review budgets, study agreements, and indemnification agreements.
• Ensure IRB approval and regulatory compliance for studies.
• Develop and maintain protocol-related documentation and tracking systems.
• Prepare and submit reports to sponsors and regulatory authorities.

Education

Bachelor’s Degree Administration

Bachelor’s Degree Business

Bachelor’s Degree Related Field

Job description

Job Description - Clinical Research Program Coordinator - Core-Ctr For Research Excel (260004E9)

Job Description

Clinical Research Program Coordinator - Core-Ctr For Research Excel - ( 260004E9 )

Description

Provides daily departmental administrative guidance and reports for conduct of new research and new sponsored projects; responsible for coordinating clinical research studies or projects which includes collaboration of new protocols, review of budgetary documents, review of institutional study agreements and indemnification agreements with study sponsors, ensuring final hospital and Institutional Review Board (IRB) approval for research studies, preparation, presentation and make recommendation for feasibility review of studies and ensure all documents are in concordance for study feasibility. Educates nurse managers/clinical nurses in reference to new studies. Coordinates activities associated with site start-up. Develops and maintains a processing and tracking systems for protocol related paperwork. Maintains an up-to-date status report and creates summary reports as requested for supervisor, PI, and/or management staff. Reviews protocols, amendments, and ancillary documents for discrepancies and/or lack of clarity. Works with PI and/or Sponsor to resolve. Prepares and submits various reports to sponsors, investigators, regulatory authorities, and Manager and any others deemed necessary. Collaboratively works with all departments to provide support for clinical trials goals.

Qualifications

Education Qualifications

• Bachelor’s Degree Administration
• Bachelor’s Degree Business
• Bachelor’s Degree Related Field

Experience Qualifications

• 3 years experience in research administration, clinical research, or project management; independent working knowledge of Clinical trial management system, electronic health record, spreadsheet and database software is required.

Primary Location

Tampa

Work Locations

TGH Main Campus 1 Tampa General Circle Tampa 33601

Eligible for Remote Work : Fully Remote

Job

Clinical Research

Schedule

Full-time

Scheduled Days : Monday, Tuesday, Wednesday, Thursday, Friday