Clinical Research Project Coordinator

About the Role

Medpace is seeking a full-time, office-based Project Coordinator to join our Clinical Trial Management team. This position will work on a team to accomplish tasks and projects instrumental to the company’s success. Therapeutic areas of focus include Microbiology, Oncology/Hematology, Cardiovascular/Metabolic/Renal, Infectious Disease/CNS/Ophthalmology, and more.

Key Responsibilities

• Engage in clinical trial management on a day-to-day level.
• Work closely with the project CTM for timely and accurate delivery of tasks.
• 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 meeting minutes.

Requirements & Tech Stack

• Excellent computer, organizational, and time management skills.

Qualifications

• Minimum of a Bachelor’s Degree in a Life Sciences field.
• Research experience preferred.

Medpace provides Project Coordinators with a 4-6 week training program that incorporates virtual and hands-on learning experience, especially for those without previous clinical research experience.