Regional Study Coordinator – Central Laboratory Services
Category: Clinical Research / Project Management
Location: Indianapolis, Indiana, United States (Hybrid)
Job Type: Full-Time
Job ID: 261116
About Labcorp
Labcorp is a global leader in life sciences and clinical research, delivering solutions that accelerate drug development and provide actionable health insights. Through its Central Laboratory Services (CCLS) network, Labcorp supports global clinical trials across Europe, Asia-Pacific, and the United States, offering over 700 assay capabilities with standardized processes, instrumentation, and quality controls.
Role Overview
Labcorp is seeking a Regional Study Coordinator (RSC) to oversee the successful execution of clinical studies within a specific region. The RSC acts as a liaison between the Global Study Manager, client representatives, and internal departments, ensuring study deliverables are met with precision and quality. This role requires strong organizational, communication, and problem-solving skills to manage local study logistics, monitoring, and supplies while maintaining alignment with global project management strategies.
This is a hybrid role based in Indianapolis, IN, combining both onsite and remote responsibilities.
Key Responsibilities
Serve as the regional liaison between Global Study Manager, clients, and CCLS departments.
Represent the Global Study Manager in interactions with client contacts when delegated.
Collaborate closely with the Global Study Manager on all study aspects, from start-up to study closure.
Review Statements of Work (SOW) to assess local feasibility and recommend operational adjustments.
Maintain detailed knowledge of SOW specifications and understand their impact on local operational execution.
Manage day-to-day local study activities, including logistics, monitoring, and study supply management.
Track and resolve local study issues, ensuring timely communication with the Global Study Manager.
Facilitate internal and occasional external meetings, providing clarity and guidance on regional study operations.
Required Education & Experience
Bachelor’s degree preferred; High School Diploma required.
Minimum 2 years of relevant clinical research or project coordination experience.
Proven ability to plan, prioritize, and manage multiple tasks in a fast-paced environment.
Strong communication, organizational, and team collaboration skills.
Attention to detail and ability to coordinate with internal teams and clients effectively.
Experience facilitating meetings and working with clients is highly desirable.
Compensation & Benefits
Pay Range: $60,000 – $65,000 per annum (based on experience and internal equity).
Employees working 20+ hours/week are eligible for comprehensive benefits including:
Medical, Dental, Vision, Life, STD/LTD coverage
401(k) Retirement Plan
Paid Time Off (PTO) or Flexible Time Off (FTO)
Tuition Reimbursement and Employee Stock Purchase Plan
Why Join Labcorp?
Work with a global leader in central laboratory services supporting clinical trials worldwide.
Gain experience in clinical trial operations, study coordination, and project management.
Collaborate with cross-functional teams and clients to ensure high-quality study delivery.
Opportunities for career growth, skill development, and exposure to international studies.
Equal Opportunity Employer
Labcorp is committed to fostering a diverse and inclusive workforce. All qualified applicants will be considered without regard to race, religion, color, national origin, sex, disability, veteran status, or any other legally protected characteristic.
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