Our global activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Database Programmer to join our Biometrics team. This position will work in 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
Develop, program, validate and maintain clinical trial databases according to company standards;
Maintain and contribute to company library of standard CDASH compliant CRFs; and
Act as primary contact to the data management team for assigned studies, supplying all necessary technical support, and ensuring quality of the programming and adherence to company standards.
Qualifications
Bachelor’s degree/Advanced degree in Life Sciences or Computer Science or equivalent;
Rave study build and/or Veeva EDC experience in a similar position in Pharma/Healthcare sector preferred;
Custom function (C# Programming) experience is preferred;
Certified Medidata Rave Study Builders preferred;
Excellent verbal and written communication skills; and
Meticulous attention to detail.
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.
Why Medpace?
When you join Medpace, you become part of an creative team that brings cutting-edge therapies to market whi