Clinical Research Coordinator
Location: Mission Valley- San Diego, California
Type: Direct Hire with client
Full Time, 40 Hours a Week
Contractor Work Model: 100% Onsite
Therapeutic Areas: Pulmonology, Dermatology, Endocrinology, Pediatrics
Compensation: $70,000 annual Role Summary
Independently manage assigned studies at the Mission Valley site with Research Assistant support. This is a hands-on role with a strong emphasis on participant recruitment, visit execution, documentation quality, and GCP compliance. Key Responsibilities
- Own day-to-day study coordination from startup through close out
- Lead patient recruitment, prescreening, and scheduling
- Conduct/coordinate study visits, informed consent, and delegated procedures (vitals, ECGs; phlebotomy preferred, including pediatric)
- Maintain source documentation, eISF/regulatory binders; support monitoring/audits
- Enter and reconcile data in EDC/CRFs; manage queries promptly
- Ensure compliance with protocol, GCP, IRB/FDA requirements; support AE/SAE reporting
- Partner with RAs to ensure visit coverage, lab processing/shipping, and timeline adherence
- Prior CRC (or equivalent site) experience; able to manage studies independently
- GCP training required
- Pediatric experience strongly preferred, pediatric phlebotomy a plus
- Experience in pulmonology/dermatology/endocrinology preferred
- Strong patient facing, documentation, and communication skills
- Comfortable in a fast paced, 100% onsite environment; recruitment is core to the role
System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.
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