Labcorp is a global leader in clinical trial services and diagnostic testing, playing a crucial role in bringing new medicines to patients worldwide. They are currently seeking talented and motivated individuals for the position of Clinical Project Coordinator (CPC).
The Clinical Project Coordinator role is an essential, high-impact entry point into the Clinical Research industry, perfect for individuals with strong organizational skills and a passion for science. If you are looking to support life-changing clinical trials, this opportunity at Labcorp is your next step.
The Clinical Project Coordinator Role at a Glance
The Clinical Project Coordinator acts as a crucial support link between the Clinical Project Manager, the investigative sites, and the sponsor. This role is primarily office-based or remote, focusing on the administrative, regulatory, and financial aspects of a clinical trial.
Key Job Details. To help candidates quickly assess their eligibility, here are the core details of this opening:
- Company: Labcorp (or its Clinical Development brand, Covance)
- Job Title: Clinical Project Coordinator (CPC)
- Loca – CPC roles are often in major hubs like RTP (NC), Princeton (NJ), or global operational centers.
- Experience: – Often 0-2 years of clinical research experience is sufficient.
- Required Education:– Typically a Bachelor’s Degree in Life Sciences, Nursing, Pharmacy, or a related health field.
- Job Type: Full-Time, [Remote, Hybrid, or On-Site]
Core Responsibilities: Driving Trial Success
The CPC role is highly involved in the day-to-day regulatory and documentation aspects of a clinical trial, ensuring all operations align with Good Clinical Practice (GCP) and regulatory guidelines.
Your primary responsibilities as a Clinical Project Coordinator will include:
- Trial Master File (TMF) Management: Maintaining, organizing, and reconciling essential regulatory documents to ensure the TMF is inspection-ready at all times. This is a crucial area for SEO keyword relevance in clinical research.
- Regulatory Support: Assisting the study teams with the preparation, submission, and tracking of regulatory documents required by global health authorities.
- Budget & Finance Tracking: Supporting the Project Manager with tracking site payment requests, invoices, and ensuring project expenditures are properly documented.
- Communication & Logistics: Serving as a central point of contact for internal teams and external site staff for non-clinical logistics and documentation issues.
- Meeting Coordination: Scheduling, organizing, and documenting internal and external project team meetings.
Essential Qualifications & Skills
Labcorp is looking for detail-oriented individuals who can manage multiple tasks efficiently. Candidates should possess the following:
Academic Credentials
- A minimum of a Bachelor’s Degree in Life Sciences, Health Administration, Biomedical Science, or equivalent education and experience.
Required Skills
- Demonstrated knowledge of Good Clinical Practice (GCP) and basic regulatory requirements is highly advantageous.
- Exceptional organizational skills and proven ability to manage time and prioritize workload effectively.
- Proficiency in MS Office Suite (Word, Excel, PowerPoint) and experience with electronic TMF systems is a plus.
- Excellent written and verbal communication skills for liaising with global teams.
Why Choose Labcorp?
Labcorp offers a robust environment for professional growth. Joining the team as a Clinical Project Coordinator provides an invaluable foundation in clinical trials, setting you up for future progression into roles such as Clinical Research Associate (CRA) or Clinical Trial Manager. Labcorp prioritizes lifelong learning and provides the necessary resources to expand your expertise in the Biopharma industry.
