Profound Research
Location
Pasadena, California
The Clinical Research Coordinator will manage all clinical trial activities under supervision, ensuring compliance with protocols, laws, and regulations. Key duties include leading trial implementation from start-up to follow-up, training staff, managing documentation, and reporting adverse events.
Candidates must meet educational requirements, such as a Bachelor's degree with 2 years of relevant experience or an Associate's degree with 4 years, along with a minimum of one year of Clinical Research Coordinator experience. Successful completion of GCP and CCRC certification within six months is mandatory, alongside experience performing clinical assessments like EKGs and blood draws.
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
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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