Clinical Research Coordinator

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

Department

Research Institute

Job Summary

Prepares and submits regulatory submission to IRB and sponsors, documentation compliance for multiple study projects, audit preparation, and data submission. This position also will be responsible for advising patients of trial design, facilitating informed consent for investigators, following strict adherence to protocol procedures specific to each study, screening for possible trial patients, eligibility criteria, and patient follow up. This position is responsible for coordination of trial activities mentioned above as well as others.

Required Qualifications

• 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..

Preferred Qualifications

• 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.

Mandatory Education

A D: Associate's Degree

Preferred Education

BD: Bachelor Degree

Employment Screening Requirements

As part of Sarasota Memorial Health Care System’s commitment to keeping people safe, all individuals providing care to vulnerable populations are required to undergo background screening through The Florida Care Provider Background Screening Clearinghouse. https://info.flclearinghouse.com/