Clinical Research Project Coordinator Job at Medpace | Apply Now
A Medpace clinical research job is now available for a full-time, office-based Project Coordinator in Cincinnati, Ohio. This role is vital for those looking to advance their careers in clinical research, particularly in the field of ophthalmology, with a focus on collaborative work and comprehensive training.
- Position: Clinical Research Project Coordinator – Ophthalmology
- Location: Cincinnati, Ohio
- Job Reference Number: 12444
About Medpace
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. Headquartered in Cincinnati, Ohio, Medpace employs more than 6,500 people across 40+ countries, focusing on accelerating the global development of safe and effective medical therapeutics through clinical research excellence.
Medpace Clinical Research Job Summary
This Medpace clinical research job is for a full-time, office-based Project Coordinator to join its Clinical Trial Management team. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. The therapeutic areas of focus include Microbiology, Oncology/Hematology, Cardiovascular/Metabolic/Renal, Infectious Disease/CNS/Ophthalmology, and more. Medpace provides Project Coordinators with a 4-6 week training program that incorporates a virtual and hands-on learning experience, especially for those without previous clinical research experience.
Eligibility Criteria
- Minimum of a Bachelor’s Degree in Life Sciences field;
- Excellent computer, organizational, and time management skills;
- Research experience preferred.
Key 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 the internal regulatory filing system;
- Manage study supplies;
- Create and maintain project timelines;
- Coordinate project meetings and produce quality meeting minutes.
Why Medpace?
When individuals join Medpace, they become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
This Medpace clinical research job, a Clinical Research Project Coordinator opportunity, is ideal for candidates looking to grow in the clinical research field. Interested individuals are encouraged to apply at the earliest to seize this chance to advance their careers in a supportive and dynamic environment.
