Clinical Research Coordinator: Trials & Compliance

Sarasota Memorial Health Care System; Sarasota (FL); On-site; USD 55,000 - 75,000; Full time

Job summary

Sarasota Memorial Health Care System is seeking a dedicated professional for the Research Institute to manage regulatory submissions, ensure protocol compliance, and coordinate multiple study projects. The role includes advising patients on trial design and facilitating informed consent for investigators, while maintaining strict adherence to study protocols.

The candidate will screen potential participants, monitor eligibility, and support data submission and audit preparation across diverse

Qualifications

• Require research certification within one year of eligibility.
• Require a minimum of five (5) years of healthcare experience with two (2) years in a research role.
• Require completion of Good Clinical Practice & Human Subject Protection and Safety Handling/Hazardous training within two weeks of hire/transfer date.

Responsibilities

• Prepare and submit regulatory submissions to IRB and sponsors, ensuring documentation compliance for multiple study projects.
• Coordinate audit preparation and data submissions for studies.
• Advise patients on trial design and facilitate informed consent for investigators.
• Screen for eligible trial patients and conduct follow-up as per protocol.
• Coordinate trial activities and other duties as assigned by the Research Institute.

Skills

Regulatory submissions

IRB processes

GCP training

Hazardous materials training

Clinical research coordination

Education

Associate's Degree

Bachelor's Degree

Job description

Sarasota Memorial Health Care System is seeking a dedicated professional for the Research Institute to manage regulatory submissions, ensure protocol compliance, and coordinate multiple study projects. The role includes advising patients on trial design and facilitating informed consent for investigators, while maintaining strict adherence to study protocols.

The candidate will screen potential participants, monitor eligibility, and support data submission and audit preparation across diverse