Responsibilities: Provides clinical research expertise in the development and conduct of day-to-day activities through all phases of a clinical trial (start up, recruitment and enrollment, data management, close out and archiving). Assists in planning, managing, implementation and reporting of clinical trials. Oversees preparation and implementation of project specific training programs and training materials for internal staff. Evaluate the resources needed vs resources available for the clinical trials running and planned. Provide strategic input aimed at ensuring continuous improvement in the way we operate and implement Standard Clinical Operating Procedures relevant to the purpose of the position. Report on status of actual vs planned recruitment from all centers participating in trials in the Country. Lead, motivate, and set objectives managing performance to assure completion of goals and development of staff. Ensure that prevailing legislation, GCP, Ethical Committee, and standard operating procedures requirements are fulfilled and monitor adherence to and compliance with standard operating procedures.