Clinical Trials Research Associate | Data & Compliance

University of South Florida

Florida

On-site

USD 65,000 - 90,000

Full time

4 days ago
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Job summary

The University of South Florida is seeking a Clinical Research Associate to support the Department of Psychiatry and Behavioral Neurosciences in Morsani College of Medicine. The role involves screening/enrollment, regulatory filing, data collection, and management of study files for clinical trials, ensuring HIPAA and institutional compliance throughout the process.

The position is onsite, Monday–Friday, grant-funded, and does not sponsor visas.

Qualifications

  • This position requires a Bachelor's degree in a field directly related to the program responsibilities and one year of professional experience; or Master's degree in an area of specialization appropriate for the program.
  • Senate Bill 1310 allows substitution of work experience for postsecondary education requirements as applicable.
  • Direct experience in clinical research, regulatory filing, and recruitment is preferred.

Responsibilities

  • Oversees screening and enrollment of participants and may supervise remote screening locations.
  • Monitors regulatory documents, informed consent, HIPAA compliance, and infection control procedures.
  • Prepares regulatory filings and IRB related materials.
  • Collects and analyzes data from clinical trials and creates databases for study information.
  • Collaborates with social workers and agencies to provide health services related to conditions.
  • Drafts program reports and provides education to clients and families about protocols.

Skills

Clinical research
Participant recruitment
Data collection & analysis
Regulatory compliance
HIPAA compliance

Education

Bachelor's degree in a related field
Master's degree in a related field

Tools

IRB submissions

Job description

The University of South Florida is seeking a Clinical Research Associate to support the Department of Psychiatry and Behavioral Neurosciences in Morsani College of Medicine. The role involves screening/enrollment, regulatory filing, data collection, and management of study files for clinical trials, ensuring HIPAA and institutional compliance throughout the process.

The position is onsite, Monday–Friday, grant-funded, and does not sponsor visas.

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