Entry-Level Research Project Coordinator

About the Role

Medpace is seeking a full-time, office-based Project Coordinator to join their Clinical Trial Management team. This role involves working on a team to accomplish tasks and projects instrumental to the company's success. The role is situated within a fast-paced, collaborative work environment focused on clinical research and career development.

Key Responsibilities

• Engage in clinical trial management on a day-to-day basis.
• Work closely with the Project CTM for timely and accurate delivery of recurrent tasks.
• Compile and maintain project-specific status reports.
• Interact with Sponsors, 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

• Bachelor’s Degree in a Life Sciences field.
• Excellent computer, organizational, and time management skills.
• Research experience preferred.

Additional Information

• Medpace provides a 4-6 week training program with virtual and hands-on learning.
• Therapeutic areas include Oncology/Hematology, Cardiovascular/Metabolic/Renal, Infectious Disease/CNS/Ophthalmology, and more.
• Medpace is a full-service clinical contract research organization (CRO).
• The role is office-based with on-site mentors and defined career paths.
• Training programs are designed to accelerate professional development.
• The environment encourages employees to influence change and contribute ideas.
• Benefits include competitive compensation, health, wellness, retirement, and PTO.
• There is potential for occasional WFH after training for eligible positions.
• Company-sponsored social events and intramural sports are available.
• The Cincinnati Headquarters offers a modern corporate campus with on-site dining, parking, and fitness facilities.