Clinical Research Associate – Recruitment & Compliance

University of South Florida; Tampa (FL); On-site; USD 70,000 - 95,000; Full time

Job summary

The University of South Florida is seeking a Clinical Research Administrator to support a health services protocol. The role involves screening/enrolling participants, developing client communications, coordinating site visits, and compiling regulatory reports.

It requires advanced knowledge and discretion, with oversight of data collection and regulatory compliance. The position may involve coordination with regulatory agencies, handling literature and educational materials for participants and

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.
• Degree Equivalency Clause: Four years of direct experience for a bachelor’s degree.

Responsibilities

• Oversees screening and enrollment of potential clients for health services protocol.
• Develops materials to communicate the project to clients and families.
• Coordinates site visits and collects data ensuring quality control.
• Maintains regulatory reports and liaises with regulatory agencies.
• Oversees clinical data gathering and ensures procedures comply with regulations.
• Monitors budgets and drafts administrative forms and reports.
• Provides education to clients and families regarding clinical protocols.
• Manages collaboration with staff and external agencies as needed.

Skills

Recruiting protocols

Regulatory compliance

Data collection

IRB knowledge

HIPAA compliance

Education

Bachelor's degree in field related to program responsibilities

Master's degree in area of specialization

Job description

The University of South Florida is seeking a Clinical Research Administrator to support a health services protocol. The role involves screening/enrolling participants, developing client communications, coordinating site visits, and compiling regulatory reports.

It requires advanced knowledge and discretion, with oversight of data collection and regulatory compliance. The position may involve coordination with regulatory agencies, handling literature and educational materials for participants and