Regional Study Coordinator - Central Labs Services - Clinical Research

Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology and laboratory network, we advance diagnostics, accelerate innovation and help address some of the world’s most important health challenges. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise, you’ll have the opportunity to do meaningful work, grow your career and make a real impact on people’s health around the world. Together, we’re improving health and improving lives.

Labcorp is seeking a hybrid Regional Study Coordinator to join our Central Labs Services team in Indianapolis.

Job Responsibilities

Serve as the regional liaison between the Global Study Manager and all CLS departments involved in study execution

Act as the regional point of contact for assigned client representatives (e.g., CRAs, Site Monitors) and the corresponding local CLS platform; may occasionally represent the Global Study Manager in interactions with primary client contacts

Partner closely with the Global Study Manager across all study stages—from start‑up through closure—to ensure seamless coordination of activities within the local platform

Review the Statement of Work (SOW) to assess local feasibility and provide informed recommendations to the Study Design Lead

Maintain deep knowledge of SOW specifications and a strong understanding of how those requirements impact operational delivery across the clinical trial

Oversee day‑to‑day local study activities, including logistics, monitoring, and study supplies, ensuring the Global Study Manager is kept informed of key developments

Monitor, track, and resolve local study issues, maintaining consistent communication with the Global Study Manager to support proactive issue management

The Regional Study Coordinator is expected to interact internally on a regular basis and occasionally with external clients throughout all job duties mentioned above.

Minimum Qualifications

High school diploma or equivalent

Two or more years of professional experience in a clinical research or laboratory setting

Preferred Qualifications

Bachelor’s degree in life science discipline

Additional Job Standards

Proven ability to plan, prioritize, and manage workload in fast‑paced, deadline‑driven environments

Strong communication and organizational skills that support clear, consistent execution

Exceptional attention to detail paired with a collaborative, team‑oriented approach

Demonstrated experience facilitating meetings and engaging effectively with clients to drive alignment and outcomes

Self‑starting, investigative mindset with the ability to learn quickly and adapt in dynamic environments

At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations.

Central Laboratory Services is part of a global contract research organization within Labcorp. We offer the world’s largest network of central laboratories and support global clinical trials testing. A common set of processes, procedures, and instrumentation is offered throughout our sites in Europe, Asia/Pacific, and the United States, allowing us to receive samples globally and provide more than 700 assays across all laboratory science disciplines.

Application Window: Closes at the end of the day September 4, 2026.

Pay Range: 60-65K

All job offers will be based on a candidate’s skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data. 

Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees are only eligible to participate in the 401(k) Plan. For more detailed information, please click here. 

Labcorp is proud to be an Equal Opportunity Employer:

Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. 

We encourage all to apply

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