Clinical project managers are responsible for organizing, communicating and evaluating team objectives for clinical studies. Their team might include clinical research associates and clinical specialists. Clinical project managers essentially plan and manage clinical trials in order to achieve quality results. They provide leadership in developing study-related documents, which might include protocols, investigator files and informed consent documents, according to MED Institute Inc. in Indiana, which identifies and develops new medical product concepts. These professionals also might have to review invoices from study vendors, institutional review board approvals, clinical study agreements and monitoring reports. Clinical project managers additionally participate in the analysis, summary and reporting of clinical data for regulatory or marketing purposes.
A project manager is a person who has the overall responsibility for the successful initiation, planning, design, execution, monitoring, controlling and closure of a project. The project manager must have a combination of skills including an ability to ask penetrating questions, detect unstated assumptions and resolve conflicts, as well as more general management skills,