Care Access
Site Manager
Lake Charles, Louisiana, United States · Principal · Full-time
No sponsorship$29k-$38kDetected 6 days ago
GCPComplianceClinical TrialsClinical ResearchFDA RegulatoryResearchLeadershipCommunicationMentoring
About the role
- About Care Access Care Access is working to make the future of health better for all.
- With hundreds of research locations, mobile clinics, and clinicians across the globe, we bring world-class research and health services directly to communities that often face barriers to care.
- To learn more about Care Access, visit www.CareAccess.com.
Responsibilities
- Directly manage and develop Clinical Research Coordinators, Phlebotomists, and Lab Technicians
- Address performance issues promptly and build a high-accountability team culture
- Lead the site's most complex and high-priority studies
- Identify operational risks and implement corrective actions to maintain study timelines
- Maintain high standards for source documentation, data integrity, and protocol compliance
- Build strong sponsor relationships through consistent, reliable execution
- Perform phlebotomy, ECGs, vital signs, and other clinical tasks
- Support informed consent processes and investigational product accountability
- Assist with additional projects such as report design, data maintenance, etc.
- Proven ability to lead, coach, and hold clinical research staff accountable for performance
Requirements
- 5+ years of clinical research experience, including time as a Clinical Research Coordinator
- Prior direct people management experience required
- Recent phlebotomy experience required
- Conduct study visits and protocol-required procedures as needed
- The Expertise Required
Compensation
- $29k-$38k
Benefits
- Partner with the Principal Investigator on operational study conduct; all medical decisions remain under PI authority
Visa & Work Authorization
- Sponsor & CRO Engagement
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This listing is sourced directly from Care Access's careers page and normalized into a canonical job model.