You will be responsible for the strategic and operational planning and management of all aspects of clinical research nurses (CRNs) including staffing, facilities, logistics and operations. You are required to co-lead clinical research study project management for the CRNs and administer clinical trial material to trial participants. You will ensure that professional nursing standards are maintained for the safety of trial participants and data collection processes are carried out according to Policies and Procedures and with integrity. Additionally, you will also adhere to Health Products Act (HPA), Human Biomedical Research Act (HBRA), safety guidelines (International Conference on Harmonisation Good Clinical Practice (ICH-GCP)) and any other applicable regulatory requirements pertaining to the management and administration of clinical trials.