Region Manager

Care Access

2d•$80,000 - $110,000•Remote

About The Position

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.

Requirements

Exceptional leadership and team-building capabilities
Excellent verbal and written communication skills
Highly organized with strong attention to detail and compliance
Proficient in Clinical Trial Management Systems (CTMS) and Microsoft Office Suite
Ability to manage multiple priorities and meet deadlines in a fast-paced environment
Ability to adapt to frequent changes in responsibilities and workloads.
Curiosity and passion to learn, innovate, able to take thoughtful risks and get things done
Friendly, outgoing personality with the ability to maintain a positive attitude under pressure
Proven ability to maintain site profitability
Minimum 5 years of clinical research experience, with 1+ years in a leadership role required
Demonstrated expertise in overseeing multiple clinical research trials across varying therapeutic areas required
Strong understanding of GCP, FDA regulations, ICH guidelines, and industry best practices required
Bachelor’s Degree preferred, or equivalent combination of education, training and experience.

Nice To Haves

Multi-site management experience preferred

Responsibilities

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 enrollment across all sites.
Lead, mentor, and support site-level teams, including Principal Investigators, Clinical Research Coordinators, and other staff.
Promote a collaborative and high-performance work culture through coaching, development, and team-building.
Proactively resolve site-level challenges and performance issues.
Ensure strict adherence to study protocols, IRB/ethics board guidelines, and applicable federal regulations.
Conduct internal site audits and oversee corrective actions when necessary.
Maintain accurate and timely documentation, including ICFs, AEs, SAEs, and source documents.
Manage site budgets and ensure adherence to financial agreements.
Support contract negotiations and oversee invoicing and payment processes.
Monitor and optimize financial performance at each site.
Collaborate with sponsors, CROs, and internal departments to ensure seamless clinical trial execution.
Monitor site performance metrics (e.g., enrollment, retention, data quality) and provide regular reports to leadership.
Oversee proper management of site resources, investigational product inventory, and study supplies.
Build and maintain strong relationships with Principal Investigators and key site personnel.
Serve as the main liaison between clinical research sites, sponsors, and internal leadership.
Advocate for site needs and promote transparency in communication across all stakeholders.
Identify and proactively address potential risks or operational issues.
Work collaboratively with internal teams to implement effective solutions and improve site efficiency.
Ability to perform the duties of a Clinical Research Coordinator and actively perform CRC responsibilities at sites as needed.