About This Role
This office-based role is for an Entry Clinical Research Project Coordinator to join the Clinical Trial Management team. The position involves working on a team to complete tasks and projects crucial to the company's success, offering an exciting career path for individuals looking to develop and grow their expertise.
Responsibilities
- Engage in clinical trial management on a day-to-day level
- Work closely with the project CTM for timely delivery of recurrent tasks consistently with a high degree of accuracy
- Compile and maintain project-specific status reports
- Update CTMS with study milestones, enrollment projections etc.
- Update eTMF and perform ongoing eTMF QC
- Support clinical trial manager to draft study plans and study specific guidance documents
- Manage site feasibility, site activation preparation and study supply managements
- Communicate with regional cross-functional team, vendors and sponsor effectively
Requirements
- Bachelor's degree in a life sciences field
- Maintain thorough knowledge of project and ability to coordinate/present at internal/external meetings and conference calls
- Excellent computer (word-processing, databases, Excel, Windows) and organizational skills
Benefits
- Competitive compensation programs that recognize and reward performance
- Comprehensive health, wellness, retirement, and PTO benefits
- Office based culture with occasional WFH that provides flexibility for eligible positions after training
- Company-sponsored social events
Application Process
A Medpace team member will review your application and if your profile matches current needs, you will be contacted for an interview. While all applications are reviewed carefully, only candidates selected for interviews will be contacted.
About the Company
Medpace is a full-service clinical contract research organization (CRO) providing phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Its mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. Medpace leverages in-country regulatory and therapeutic expertise across all major therapeutic areas, including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, it employs more than 6,500 people across 40+ countries.
