Clinical Trial Pharmacist Cancer & Blood Research

Exciting opportunity within Cancer and Blood Research, a fast‑growing team involved in local and international research! Expert knowledge with the ability to make a difference in research for people with cancer. About the Role Te Pūriri o Te Ora – Auckland’s Regional Cancer and Blood Service based at Auckland City Hospital is the leading provider of cancer care in the Auckland region, serving a large and varied population of around 1.7million people. Cancer and Blood Research offers people with cancer and their whānau the opportunity to participate in high‑quality clinical, translational and observational research, leading to improved clinical outcomes. You will be joining a busy, dynamic and diverse team of clinical research professionals striving to ensure that novel therapies and clinical trials are available to our patient population both here in Auckland and across NewZealand. As the clinical trials pharmacist, you will be an integral part of our operational team and will manage day‑to‑day research pharmacy activities across a number of commercial and investigator‑led trials. The role requires close liaison with Auckland City Hospital clinical pharmacy services, commercial sponsors and monitors, and external pharmacy and compounding sites. Key responsibilities include: Providing expertise in the set‑up aspects of clinical trials, including study feasibility, draft electronic script preparation, dispensing guide, and knowledge of e‑pharmacy software in compliance with ICH‑GCP and NewZealand pharmaceutical regulators. Managing day‑to‑day research pharmacy activities across commercial and investigator‑led trials. Collaborating closely with hospital clinical pharmacy services, commercial sponsors, monitors, and external pharmacy and compounding sites. About you To be successful in this role, you will hold relevant pharmacy qualifications and registration and have proven experience working in a clinical trials pharmacy. Knowledge of NZ regulators for drug trials and ICH‑GCP and application to drug trial management is also essential. You will also need to be committed to biculturalism and achieving equitable outcomes for Māori. Ideally, you will have previous experience working in DHBs and have people‑management or supervisory skills. #J-18808-Ljbffr