Clinical Research Program Coordinator - Core-Ctr For Research Excel

Florida Health Sciences Center Tampa General Hospital; Tampa (FL); Remote; USD 52,000 - 78,000; Full time

Benefits offered by this job

Fully remote eligibility

Job summary

Tampa General Hospital, Inc. is seeking a Clinical Research Program Coordinator for the Core-Ctr For Research Excel to manage daily departmental guidance and coordinate new studies and sponsored projects.

You will review budgets, study agreements, and regulatory documents while ensuring IRB approvals and feasibility assessments. The role involves site start-up activities, maintaining protocol documentation, and close collaboration with investigators, sponsors, and hospital departments to advance

Qualifications

• 3 years experience in research administration, clinical research, or project management.
• Experience with clinical trial management systems and electronic health records is expected.
• Ability to review budgets, study agreements, and regulatory documents.

Responsibilities

• Coordinate clinical research studies and projects.
• Review budgetary documents and study agreements with sponsors.
• Ensure IRB approval and regulatory compliance for studies.
• Prepare feasibility reviews and maintain status/tracking of protocol paperwork.
• Educate staff on new studies and support site start-up activities.
• Generate reports for supervisor, PI, and management.

Skills

Clinical research coordination

Project management

Education

Bachelor’s degree in Administration

Bachelor’s degree in Business

Bachelor’s degree in Related Field

Tools

CTMS

EHR

Excel

Databases

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