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 that data collection processes are carried out according to Policies and Procedures with integrity. Additionally, you will also adhere to the 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.

• Degree in Nursing with Advanced Diploma in Nursing or equivalent
• Relevant experience ...