A BDN client is looking for a Clinical Program Manager for a 3-6 month temporary to perm opportunity. This person will facilitate study design by working with the Chief Scientific Officer. This is a highly visible role that will be responsible for designing, drafting, and establishing study protocols, case reports, informed consent reports, study master files, and other documentation for clinical studies supporting product development. Other responsibilities include: leading process for IRB approvals, initiating, monitoring, and conducting study close out procedures at clinical study centers. Executing clinical studies, including leading clinical study data, status, and final study reports are needed. 5 or more years of experience with clinical trials in an industry setting, with at least 1 year in project/program management is preferred. Direct experience managing complex In Vitro Diagnostic clinical studies or infectious disease studies is a definite plus. A Bachelor's Degree in Nursing or related field is essential to this role.