We are currently seeking a full time, office-based Clinical Research Project Coordinator Entry to join our Clinical Trial Management team in Navi Mumbai, India. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.
Responsibilities
Engage in clinical trial management on a day to day level;
Work closely with the project CTM for timely delivery of recurrent tasks consistently with a high degree of accuracy;
Compile and maintain project-specific status reports;
Update CTMS with study milestones, enrolment projections etc.
Update eTMF and perform ongoing eTMF QC;
Support clinical trial manager to draft study plans and study specific guidance documents;
Manager site feasibility, site activation preparation and study supply managements;
Communicate with regional cross functional team, vendors and sponsor effectively;
Qualifications
Bachelor's degree in a life sciences field;
Maintain thorough knowledge of project and ability to coordinate/present at internal/external meetings and conference calls;
Excellent computer (word-processing, databases, Excel, Windows) and organizational skills.
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical research. We leverage 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. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.