Overview:
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.
Responsibilities:
* Manage multiple projects from am eClinincal/eCOA perspective;
* Develop and review study documentation related to eClinical/eCOA activities for clinical trials with sponsor companies and other departments;
* Coordinate overall eClinical activities by serving as primary contact for the sponsor;
* Monitor study timelines in relation to clinical trial needs;
* Attend face to face sponsor meetings and Investigator Meetings
Qualifications:
* Bachelor's degree and prior eClinical experience; including setting up and managing multiple eClinical/eCOA projects and acting as the main point of contact for the sponsor;
* General knowledge of technology trends and system / application development;
* Possess excellent organizational, prioritization, and time management skills;
* A basic knowledge of medical terminology is needed, as well as knowledge of a scientific investigative methodologies and clinical research methodologies.
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