Clinical Research Coordinator (San Diego, CA)*

As a Clinical Research Coordinator I at Profound Research, you’ll serve as the primary coordinator for assigned studies at one of our sites. You’ll manage study activities from start-up through closeout, lead interactions with study participants, maintain audit-ready documentation, and work directly with investigators, sponsors, and CROs. This isn’t a support role – you own your studies, and your work directly impacts patient safety, data integrity, and trial outcomes. 

What You’ll Do

• Serve as primary coordinator for assigned clinical trials, managing study activities from start-up through closeout

• Execute full visit flow independently – participant visits, protocol procedures, data collection, and documentation

• Lead patient interactions with clarity and compassion, ensuring participants feel informed and supported throughout their study experience

• Maintain accurate, timely, audit-ready documentation across source documents, CRFs, and EDC systems

• Key Requirements & Skills

  • Communicate directly and professionally with investigators, sponsors, CROs, and internal teams

  • Support site readiness for monitoring visits and audits

  What We’re Looking For

  You’ve got some experience in clinical research and you’re ready for more responsibility. You’re organized, detail-oriented, and comfortable working independently. You take ownership of your work and follow through without being reminded. 

  • Bachelor’s degree with 1+ year of relevant experience, OR Associate’s degree with 3+ years of relevant experience, OR High school diploma with 4+ years of relevant experience and at least 1 year of CRC experience