Clinical Research Project Coordinator - Ophthalmology

Medpace•Cincinnati, OH

30d•Onsite

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 areas of focus include Microbiology, Oncology/Hematology, Cardiovascular/Metabolic/Renal, Infectious Disease/CNS/Ophthalmology and 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