We are currently seeking a full-time, office-based Clinical Research 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. 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 health sciences field;Prior experience as a Study Coordinator or within the pharmaceutical industry; andExcellent computer (word-processing, databases, Excel, Windows), organizational, and communication skills. Medpace OverviewMedpace 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.
Why Medpace?When you join Medpace, you become part of a team dedicated to supporting the development of ground-breaking drugs and devices. Our employees provide hope for those living with debilitating diseases. We invite you to be a part of something that is impacting millions of people around the globe while enjoying a competitive total compensation and benefits package and internal growth opportunities.
Awards:
Medpace historically named a Top Cincinnati Workplace by the Cincinnati EnquirerMedpace ranks amongst top CROs for site ratings across all 10 important attributes including CRA training, preparation & organization, accessibility of staff, open communication, and ensuring timely drug availability Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibilityWhat to Expect Next:
A member of our recruitment team will review your qualifications and, if interested, you will be contacted for an interview.
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