Clinical Research Project Coordinator - Oncology

Medpace•Cincinnati, OH

31d•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 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. Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Requirements

Minimum of a Bachelor's Degree in Life Sciences field
Excellent computer, organizational, and time management skills
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