Clinical Research Project Coordinator
Medpace
About the Role
Medpace is seeking a full-time, office-based Project Coordinator to join our Clinical Trial Management team, specializing in Infectious Disease. This role is instrumental to the company’s success within a fast-paced, collaborative work environment in clinical research.
Key Responsibilities
- Engage in clinical trial management on a day-to-day level.
- Work closely with the project CTM for timely delivery of tasks with high accuracy.
- Compile and maintain project-specific status reports.
- Interact with the Sponsor, study sites, and internal associates.
- Provide oversight and quality control of the internal regulatory filing system.
- Manage study supplies.
- Create and maintain project timelines.
- Coordinate project meetings and produce quality meeting minutes.
Requirements & Tech Stack
- Bachelor’s Degree in a Life Sciences field.
- Excellent computer skills.
- Excellent organizational skills.
- Excellent time management skills.
- Research experience preferred.
Training
Medpace provides a 4-6 week training program that incorporates virtual and hands-on learning.