Clinical Research Project Coordinator Job at Medpace | Apply Now
A full-time, office-based Medpace Project Coordinator opportunity is available in Cincinnati, Ohio. This role is pivotal in the Clinical Trial Management team, focusing on various therapeutic areas. Interested candidates are encouraged to apply promptly.
Medpace Project Coordinator Job Details
- Position: Clinical Research Project Coordinator – Immunology
- Location: Cincinnati, Ohio
- Department: Clinical Trial Management
- Reference Number: 12359
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. The organization is committed to accelerating the global development of safe and effective medical therapeutics through the advancement of clinical research. Headquartered in Cincinnati, Ohio, Medpace employs more than 6,500 people across over 40 countries, leveraging 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.
Medpace Project Coordinator Responsibilities
The Coordinator will work as part of a team to accomplish tasks and projects that are instrumental to the company’s success. This position is ideal for those looking to develop their career in a collaborative environment within clinical research. Medpace offers a comprehensive 4-6 week training program, especially beneficial for candidates without previous clinical research experience.
Eligibility Criteria
- Minimum of a Bachelor’s Degree in a Life Sciences field;
- Excellent computer, organizational, and time management skills;
- Research experience preferred.
Medpace Project Coordinator – 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?
- Become part of an innovative team dedicated to bringing cutting-edge therapies to market.
- Foster a meaningful career focused on scientific excellence and improving patient outcomes.
- Engage in continuous learning and cross-functional collaboration.
Medpace is offering a compelling opportunity for qualified candidates to join their team as a Clinical Research Project Coordinator. Interested individuals are encouraged to apply at the earliest to ensure they do not miss out on this chance to advance their careers in clinical research.
