Opportunities

Our Clinical Research and Pharmacovigilance team pushes the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe, effective, innovative medicine.

This role is responsible for comprehensive trial and site administration. Under the oversight of the Clinical Trial Coordinator Manager, the person prepares, collates, distributes, and archives clinical documents. The Clinical Trial Coordinator (CTC) supports clinical supply & non-clinical supply management and ensures timely maintenance of tracking and reporting tools, as applicable. The role is critical to meet planned Site Ready dates, including assisting with the preparation of submission packages to the Internal Review Board / Ethics Review Committee and Health Authorities. The role will collaborate at the local level closely with Clinical Operations Manager (COM), Clinical Research Manage (CRM) and Clinical Research Associate (CRA).