Description
The Medical Director, Oncology Clinical Development is a physician who brings medical expertise, clinical judgement, and a patient-centred perspective to the design, conduct, and interpretation of clinical studies.
In this role, you will serve as the physician within the clinical program team, providing medical expertise across study design, conduct, safety oversight, and data interpretation.
Key responsibilities include:
- Leading medical monitoring activities for clinical studies, ensuring patient safety, clinical integrity, and compliance with the protocol and regulatory requirements
- Interpreting clinical and safety data from a physician perspective, generating insights that inform study-level and program-level decisions
- Partnering with the Senior Scientist and cross-functional teams to ensure medical considerations are integrated into study execution and delivery
- Contributing medical expertise to protocol development, ensuring clinical relevance, patient safety, and feasibility
- Serving as a core member of the Clinical Matrix Team (CMT), providing the medical voice in study-level discussions and cross-functional decision-making
This role requires an MD (or equivalent medical degree) with board certification or eligibility in oncology, hematology, or hematology oncology, as well as experience in treating patients with clonal myeloid disorders.
The ideal candidate will have experience in clinical trial conduct, including medical monitoring, safety review, and clinical data interpretation, as well as experience leading or supporting clinical development activities in accordance with GCP and ICH guidelines and global regulatory frameworks.