Clinical Research Project Coordinator - Oncology
About The Position
Medpace is a leading CRO for Biotech companies and we are currently 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 that are instrumental to the company’s success. Our therapeutic area of focus includes Oncology/Hematology, among many more. If you are looking for a fast paced, collaborative work environment in clinical research and want to develop your career even further, then this is the opportunity for you. Medpace provides Project Coordinators a 4-6 week training program that incorporates a virtual and hands on learning experience, especially for those without previous clinical research experience.
Requirements
- Minimum of a Bachelor’s Degree in Life Sciences field
- Excellent computer, organizational, and time management skills
Nice To Haves
- Research experience preferred
Responsibilities
- Engage in clinical trial management on a day to day level
- Work closely with the project CTM for timely delivery of tasks consistently with a high degree of accuracy
- Compile and maintain project-specific status reports
- Interact with the Sponsor, study sites, and internal associates
- Provide oversight and quality control of our internal regulatory filing system
- Manage study supplies
- Create and maintain project timelines
- Coordinate project meetings and produce quality meeting minutes
Benefits
- Competitive compensation programs that recognize and reward performance
- Comprehensive health, wellness, retirement, and PTO benefits
- Company-sponsored social events and intramural sports
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
