Clinical Research Coordinator — IRB & GCP

Sarasota Memorial Health Care System; Sarasota (FL); On-site; USD 60,000 - 90,000; Full time

Job summary

Sarasota Memorial Health Care System is seeking a Research Coordinator to prepare and submit regulatory submissions to IRB and sponsors, ensuring strict documentation compliance across multiple study projects.

The role includes coordinating audit activities, advising patients on trial design, and facilitating informed consent while screening for eligible participants and coordinating trial activities. Strong GCP knowledge and healthcare experience are required.

Qualifications

• Certification in research within 1 year of eligibility.
• Minimum 5 years healthcare experience with 2 years in a research role.
• Complete GCP, Human Subject Protection and Hazardous Training within 2 weeks of hire.

Responsibilities

• Prepare and submit regulatory submissions to IRB and sponsors.
• Ensure documentation compliance for multiple study projects.
• Assist with audit preparation and data submission.
• Advise patients on trial design and facilitate informed consent.
• Screen for eligible trial patients and coordinate trial activities.

Skills

Research certification

Healthcare experience

GCP training

Education

Associate's Degree

Bachelor's Degree

Job description

Sarasota Memorial Health Care System is seeking a Research Coordinator to prepare and submit regulatory submissions to IRB and sponsors, ensuring strict documentation compliance across multiple study projects.

The role includes coordinating audit activities, advising patients on trial design, and facilitating informed consent while screening for eligible participants and coordinating trial activities. Strong GCP knowledge and healthcare experience are required.