Clinical Research Coordinator: Trials & Compliance Lead

Golden State Dermatology; Walnut Creek (CA); On-site; USD 55,000 - 83,000; Full time

Job summary

Golden State Dermatology in Walnut Creek, CA is seeking a Clinical Research Coordinator to support conduct of clinical trials under PI direction. This role requires coordinating regulatory activities, participant recruitment, data entry in EDC, safety reporting, and ensuring adherence to GCP and FDA regulations.

The coordinator will collaborate with investigators, sponsors, CROs, and study staff, travel to Walnut Creek sites as needed, and contribute to study milestones from start-up through

Qualifications

• Bachelor’s degree or equivalent required.
• At least 2 years of clinical research experience.
• Experience with sponsors and CROs preferred.
• Working knowledge of ICH‑GCP and FDA regulations.
• Travel frequently to Walnut Creek site.

Responsibilities

• Support study feasibility and start-up activities.
• Coordinate day‑to‑day activities for clinical studies.
• Recruit, prescreen, enroll, and retain participants.
• Enter data into EDC systems and ensure data quality.
• Prepare study documentation and regulatory submissions.
• Monitor study progress and communicate with sponsors and sites.
• Assist with study close-out and archiving.

Skills

Communication

Organization

Problem‑solving

Willingness to travel

Education

BA/BS or equivalent

Tools

EDC systems

MS Office

Google Workspace

Job description

Golden State Dermatology in Walnut Creek, CA is seeking a Clinical Research Coordinator to support conduct of clinical trials under PI direction. This role requires coordinating regulatory activities, participant recruitment, data entry in EDC, safety reporting, and ensuring adherence to GCP and FDA regulations.

The coordinator will collaborate with investigators, sponsors, CROs, and study staff, travel to Walnut Creek sites as needed, and contribute to study milestones from start-up through