Clinical Research Coordinator (San Diego, CA)*
Profound Research·Carlsbad, California
Profound Research·Carlsbad, California
The Clinical Research Coordinator manages all clinical trial activities, including study start-up, subject recruitment, and data collection in compliance with protocols and regulations. They also mentor staff and ensure accurate documentation and reporting of adverse events.
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
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.
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Candidates must have a degree in the life science industry with relevant experience ranging from 2 to 6 years depending on the degree level. Proficiency in clinical assessments and a commitment to obtaining GCP and CCRC certifications are required.
Market context
In California, physician openings are typically driven by ongoing demand across large health systems, outpatient groups, and specialty practices, with competition shaped by board eligibility, licensure, and specialty fit. For this role category, candidates are often compared on clinical experience, communication skills, and readiness to work within team-based care. The job requirements and benefits on this platform are AI-summarized from the original job description, saving candidates research time. Review the CPT and BLS requirements carefully and confirm your experience aligns with the listed laboratory and acute-care expectations before applying.
