Clinical Research Site Manager
$100,000–$105,000 year
On-site · Riverside, California, United States
Job Summary
Site Manager at Headlands Research overseeing both clinical research coordination and site operations, accountable for meeting enrollment KPIs and financial targets, mentoring staff (CRC, RAs, administrative personnel, RNs), ensuring regulatory compliance (FDA, ICH, GCP), and coordinating with HR for hiring. Responsibilities include maintaining study calendars, monitoring enrollment, supervising staff, ensuring quality documentation (CTMS, regulatory forms), overseeing trial initiation and execution, and optimizing patient recruitment and retention while upholding participant safety and rights.
Required Qualifications
- 5+ years of experience as a delegated Clinical Research Coordinator on multiple phase 2-4 clinical research trials, simultaneously
- Proficiency in FDA regulations governing clinical trials
- Strong supervisory skills to lead research staff effectively
- Ability to collect and manage research data accurately
- Familiarity with documentation review processes in clinical research
- Knowledge of medical terminology relevant to clinical trials management
- IATA (dangerous goods handling)
- GCP (Good Clinical Practice)
- Strong communication skills with all members of the team.
Apply with one swipe on Sorce. We auto-fill applications and apply on your behalf — no cover letters, no 40-minute forms.
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.