Regional Study Coordinator - Central Labs

Labcorp; Indianapolis (IN); Remote; USD 60,000 - 65,000; Part time

Benefits offered by this job

401(k) Plan

Medical, Dental, Vision

Paid Time Off (PTO)

Tuition Reimbursement

Employee Stock Purchase Plan

Job summary

Labcorp is seeking a Regional Study Coordinator to manage clinical studies in a remote setting across the US. The role involves being the primary liaison between teams and ensuring successful delivery of operations while monitoring contractual obligations. Candidates should have strong communication and organizational skills, along with relevant experience in the field.

Qualifications

• At least two years of applicable experience.
• Demonstrated ability to plan and prioritize tasks in a fast-paced environment.
• Exceptional communication and organizational skills.

Responsibilities

• Act as regional liaison between Global Study Manager and various departments involved in the study.
• Review the study Statement of Work to ensure local feasibility.
• Manage day-to-day local study activities and monitor study issues.

Skills

Communication

Organizational skills

Attention to detail

Teamwork

Education

Bachelor's degree preferred

High School Diploma required

Job description

Regional Study Coordinator - Central Labs

Join to apply for the Regional Study Coordinator - Central Labs role at Labcorp

Regional Study Coordinator - Central Labs

Join to apply for the Regional Study Coordinator - Central Labs role at Labcorp

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.

The Regional Study Coordinator (RSC) is responsible for the successful delivery of all operations of a clinical study in their specific area of the world. The RSC acts as the appointed liaison between the Global Project Management department, client representatives, and other departments involved in the clinical study to ensure the successful management of regional study responsibilities. The Regional Study Coordinator may communication with the client directly when a task is being delegated by the Global Study Manager. Regular communication is essential with the appointed Global Study Manager who is accountable for the entire protocol. This position must follow the Central Labs Global Project Management strategy and deliver outstanding customer satisfaction and performance.

This is a remote opportunity and can be located anywhere in the US.

Responsibilities

• Act as regional liaison between Global Study Manager and various CCLS departments involved in the study
• Act as regional liaison between assigned Client representatives (eg. CRA, Site Monitors) and the corresponding local CCLS platform; occasionally, the Regional Study Coordinator can represent Global Study Manager in interactions with the main client contact
• Close collaboration with the Global Study Manager for all study related aspects that are pertaining to the corresponding local platform and through all study stages, from set-up to closure
• Review the study Statement of Work to ensure local feasibility and make appropriate recommendations to the Study Design Lead
• Ensure a detailed knowledge of the SOW specifications and very good understanding of how the SOW specifications impact every operational aspect of the clinical trial
• Manage day-to-day local study related activities, especially logistics, monitoring and study supplies, keeping the Global Study Manager informed of any study development
• Monitor, track and provide resolution to all local study issues, keeping the Global Study Manager in the communication loop
  
  

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

Experience And Qualifications

• Bachelor's degree preferred; High School Diploma required
• At least two years of applicable experience
• Demonstrated ability to plan and prioritize tasks and workload in a fast-paced environment
• Exceptional communication and organizational skills
• Excellent attention to detail and teamwork orientation
• Demonstrated ability to facilitate meetings and work with clients
  
  

Application Window: The application window will close at the end of the day on July 4, 2025.

Work Location: US Remote

Pay Range: 60-65K per annum

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. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. 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

If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Part-time

Job function

• Job function

  Research, Analyst, and Information Technology

• Industries

  Hospitals and Health Care

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