Care Access
Healthcare
RegionManager
Neural analysis suggests this role is
optimal for Manager candidates.
“Region Manager at Care Access. Skills: Clinical trial execution, Site management, Regulatory guidelines. Oversee day-to-day operations. Ensure trials compliance”
What You'll Achieve.
Maintain site profitability
Industry & Context.
Resolve challenges; Resolve issues; Address risks; Address operational issues; Implement solutions
Up to 50% travel, On site monthly, Use keyboards, Use computer equipment, Walking, Standing, Sitting, Lifting up to 25lbs, Lifting overhead, Driving 20%
What They're Looking For.
Must Have
Minimum 5 years clinical research experience, 1+ years leadership role experience, Multi-site management experience, Expertise overseeing multiple clinical trials, Understanding of GCP, Understanding of FDA regulations, Understanding of ICH guidelines, Understanding of industry best practices
Nice to Have
Bachelor's Degree preferred, Equivalent combination of education, training and experience
What You'll Do.
Oversee day-to-day operations
Ensure trials compliance
Lead clinical trial execution
Ensure data collection quality
Ensure timely patient enrollment
Lead site-level teams
Promote collaborative work culture
Resolve site-level challenges
Resolve performance issues
Ensure adherence to protocols
Ensure adherence to IRB guidelines
Ensure adherence to federal regulations
Conduct internal site audits
Oversee corrective actions
Maintain accurate documentation
Ensure adherence to financial agreements
Support contract negotiations
Oversee invoicing processes
Oversee payment processes
Monitor financial performance
Collaborate with sponsors
Collaborate with CROs
Collaborate with internal departments
Monitor site performance metrics
Provide regular reports
Oversee resource management
Oversee investigational product inventory
Oversee study supplies management
Build relationships with Principal Investigators
Build relationships with site personnel
Advocate for site needs
Promote transparency in communication
Identify potential risks
Address operational issues
Implement effective solutions
Improve site efficiency
Perform CRC responsibilities
How You'll Work.
Team & Collaboration
Cross-functional teams; Internal departments; Sponsors; CROs
Communication Scope
Verbal communication; Written communication
Full Job Description
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. We are dedicated to ensuring that every person has the opportunity to understand their health, access the care they need, and contribute to the medical breakthroughs of tomorrow. With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Through partnerships, technology, and perseverance, we are reimagining how clinical research and health services reach the world. Together, we are building a future of health that is better and more accessible for all. To learn more about Care Access, visit www.CareAccess.com. How This Role Makes a Difference We are seeking an experienced and dynamic Region Manager to lead the operations and performance of multiple clinical research sites. This role is critical in ensuring the successful execution of clinical trials in accordance with regulatory guidelines, timelines, and quality standards. The ideal candidate is a results-driven leader with deep clinical research experience, strong regulatory knowledge, and a passion for team development, patient care, and operational excellence. How You'll Make An Impact Site Operations & Oversight Oversee day-to-day operations at multiple clinical research sites within the region. Ensure trials are conducted in full compliance with Good Clinical Practice (GCP), FDA, ICH, and protocol requirements. Lead all phases of clinical trial execution including site initiation, monitoring, subject recruitment, and study close-out. Ensure consistent, high-quality data collection and timely patient e
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