Clinical Trials Regulatory Coordinator

Sarah Cannon Research Institute; Nashville (TN); On-site; USD 65,000 - 90,000; Full time

Job summary

Sarah Cannon Research Institute seeks a Regulatory Coordinator in Nashville, TN. This role manages regulatory affairs compliance, documents, and site start-up support across networks.

You'll ensure FDA/GCP documentation is current and aligned with SOPs, coordinating with investigators and operations teams. The successful candidate will have an associate degree (bachelor preferred) and regulatory or customer service experience.

Qualifications

• Associate degree or higher required; bachelor’s preferred.
• Regulatory experience is preferred.
• Customer service experience is preferred.

Responsibilities

• Manage regulatory affairs compliance for sponsors/sites and ensure deadlines are met.
• Process regulatory document signatures and maintain electronic signatures and file systems.
• Maintain FDA and GCP documentation for sites, studies, sponsors and networks.
• Triage site regulatory support requests and establish correct pathways for issue resolution.

Skills

Regulatory experience

Customer service experience

Associate degree

Education

Associate Degree, preferably a Bachelor’s Degree

Job description

Sarah Cannon Research Institute seeks a Regulatory Coordinator in Nashville, TN. This role manages regulatory affairs compliance, documents, and site start-up support across networks.

You'll ensure FDA/GCP documentation is current and aligned with SOPs, coordinating with investigators and operations teams. The successful candidate will have an associate degree (bachelor preferred) and regulatory or customer service experience.