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Posted 21 hours ago
Clinical Research Site Manager
Headlands ResearchClinical Research Site Manager
Requirements
5+ years Clinical Research Coordinator experience, FDA regulations proficiency, Supervisory skills, IATA certification, GCP knowledge
Skills
Clinical ResearchGCPFDA Regulations
About the role
Responsibilities
- Evaluate site performance and implement process improvements
- Manage site calendar, enrollment targets, and employee PTO
- Hire, train, and mentor site staff including Coordinators and Nurses
- Ensure compliance with FDA, ICH, and local regulatory guidelines
- Perform Clinical Research Coordinator duties including protocol execution
- Manage patient recruitment, retention, and eligibility assessments
- Maintain study records, case report forms, and CTMS documentation
Requirements
- 5+ years of experience as a Clinical Research Coordinator on phase 2-4 trials
- Proficiency in FDA regulations governing clinical trials
- Strong supervisory and leadership skills
- Knowledge of medical terminology and documentation review
- IATA certification
- GCP (Good Clinical Practice) certification
- Strong communication skills
Preferred Qualifications
- Bachelor's degree
- Phlebotomy capability
- CCRC or CCRP certification
About the Company
Headlands Research is a leading network of advanced clinical trial sites dedicated to enhancing clinical trial delivery through cutting-edge technology and exceptional support services.
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Headlands Research · Riverside
