Clinical Research Coordinator (San Diego, CA)*

About Profound Research  Profound Research partners with community physicians to offer clinical trials as a therapeutic option for their patients. We handle all infrastructure, regulatory compliance, and administrative operations so physicians can focus on patient care. Our model gives patients access to the newest therapies while maintaining the trusted patient-physician relationship.     Our Mission: Improving Lives by Providing Advanced Therapeutic Options    Our Vision: Creating the Absolute Best Patient-Physician Experience in Clinical Research    Our Values:   Compassion: We prioritize the patient-physician relationship, ensuring every interaction is service-oriented and patient-centered.  Urgency: We work hard and practice selflessness, acting swiftly and decisively to meet the needs of our patients, partners, and colleagues.   Solution Orientation: We embrace challenges with a positive mindset, communicate directly, and identify and implement effective solutions with efficiency.   Excellence: We insist on excellence, holding ourselves accountable and empowering each other to deliver best-in-class service while maintaining the highest ethical and scientific standards.   Own Your Studies. Grow Your Career.  If you’re ready to step into real ownership of clinical trial coordination – managing your own studies, leading patient visits, and working with the independence that comes from having built a strong foundation – this role is the next step.     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