Senior Clinical Research Coordinator

As a Senior Clinical Research Coordinator at Artemis Institute for Clinical Research, you will be responsible for managing multiple phase 2-4 industry-sponsored clinical trial studies, providing high-level care for study patients, and delivering excellent customer service to pharmaceutical clients. You will work in a collaborative, clinical environment and be part of a team that values strong operations, multidisciplinary collaboration, and a schedule that supports work-life balance.

What You Will Do

Your main responsibilities will include coordinating all aspects of assigned clinical trials from site initiation through close-out, conducting subject visits, and ensuring accurate, timely documentation in compliance with protocol and standards. You will also manage subject recruitment, informed consent, and retention activities, and ensure timely EDC data entry and resolution of queries.

Why It Might Be a Fit

This role is ideal for CRCs who enjoy owning their studies, working with competent teams, and being trusted to execute with precision. You will have the opportunity to work on complex, meaningful studies, and be part of a growing research network with resources and stability.

Requirements

• At least two years of experience managing multiple phase 2-4 industry-sponsored clinical trial studies as the primary coordinator
• High school diploma or GED
• Strong understanding of FDA regulations, ICH-GCP, and clinical trial operations
• Experience with EDC, IVRS, and clinical research platforms
• Proficiency in medical terminology and clinical documentation
• Strong organizational skills with the ability to manage multiple studies
• Clear, professional verbal and written communication skills

Benefits

• California Pay Range: $85,000—$90,000 USD