Entry-Level Study Start-Up Coordinator
Medpace, Inc.•Cincinnati, OH
•Onsite
About The Position
Our clinical operations activities are growing rapidly, and we are currently seeking full-time, office-based Study Start-Up Coordinators to join our Regulatory Submissions team. In this position you will work independently and collaboratively to manage timelines, meet goals, and play a key role in the clinical trial management and study start-up process at Medpace. If you are seeking an exciting, entry-level position where you can build a foundation in the clinical research industry and develop/grow your career through our robust training program, then this is the opportunity for you.
Requirements
- Bachelor's degree is required (Life Sciences field preferred)
- Some experience in an office setting is preferred
- Excellent organizational and prioritization skills
- Knowledge of Microsoft Office
- Great attention to detail and excellent oral and written communication skills
Responsibilities
- Communicate with research sites (doctor's offices, universities, hospitals, etc.) to collect all essential documents required before the site begins to screen patients to participate in the clinical trial
- Maintain and perform ongoing quality review of trial documents within the Trial Master File (TMF)
- Collect, review, organize, and assemble regulatory start-up submissions (includes submissions to Institutional Review Boards)
- Maintain timelines for study start-up through internal team collaboration
Benefits
- Comprehensive health, wellness, retirement, and PTO benefits
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
