Clinical Research Coordinator

Sarasota Memorial Health Care System • Sarasota, FL

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About The Position

This position is responsible for preparing and submitting regulatory submissions to the IRB and sponsors, ensuring documentation compliance for multiple study projects, preparing for audits, and submitting data. The role involves advising patients on trial design, facilitating informed consent for investigators, strictly adhering to protocol procedures for each study, screening for potential trial patients based on eligibility criteria, and conducting patient follow-up. The Clinical Research Coordinator is responsible for the overall coordination of trial activities.

Requirements

• Require research certification within one (1) year of eligibility.
• Require a minimum of five (5) years of healthcare experience with two (2) of the years being within a research role.
• Require completion of Good Clinical Practice & Human Subject Protection and Safety Handling/Hazardous training within two (2) weeks of hire/transfer date.

Nice To Haves

• Prefer in-depth knowledge of good clinical practices as set forth by Federal regulations.
• Prefer an organized individual with strong critical thinking skills who has the ability to work efficiently under pressure.
• Prefer someone who is highly motivated, shows initiative, is proactive, and able to work independently as well as in a team.

Responsibilities

• Prepares and submits regulatory submission to IRB and sponsors
• Ensures documentation compliance for multiple study projects
• Prepares for audits
• Submits data
• Advises patients of trial design
• Facilitates informed consent for investigators
• Follows strict adherence to protocol procedures specific to each study
• Screens for possible trial patients based on eligibility criteria
• Conducts patient follow-up
• Coordinates trial activities

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Associate degree