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CARE

Region Manager

CARE

Region Manager overseeing operations of multiple clinical research sites to ensure successful execution of clinical trials. Leading teams and ensuring compliance across all phases of clinical trials.

Posted 6/10/2026full-timeRemote • 🇺🇸 United StatesMid-LevelSenior💰 $80,000 - $110,000 per yearWebsite

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • 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.
  • 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.

Requirements

What you’ll need
  • Minimum 5 years of clinical research experience, with 1+ years in a leadership role required
  • Multi-site management experience preferred
  • 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.

Benefits

Comp & perks
  • Paid Time Off (PTO) and Company Paid Holidays
  • 100% Employer paid medical, dental, and vision insurance plan options
  • Health Savings Account and Flexible Spending Accounts
  • Bi-weekly HSA employer contribution
  • Company paid Short-Term Disability and Long-Term Disability
  • 401(k) Retirement Plan, with Company Match

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools
clinical researchdata collectionsite initiationmonitoringsubject recruitmentstudy close-outsite auditsbudget managementcontract negotiationsperformance metrics
Soft Skills
leadershipmentoringteam-buildingcollaborationproblem-solvingcoachingcommunicationorganizational skillsperformance managementdevelopment