Medical Director

The client is seeking an experienced clinical development physician to take on the role of Medical Director for early-stage oncology trials. This position involves authoring clinical protocols and various regulatory documents, including clinical study reports and training materials. Key responsibilities include performing medical and safety/efficacy data reviews, preparing trial result summaries for various stakeholders, managing drug safety activities, and supporting clinical site initiation visits. The role requires a deep understanding of oncology, strong clinical judgment, and effective collaboration with global teams and external partners. Candidates must possess an MD, MD/PhD, or advanced clinical degree with at least 5 years of clinical development experience in the industry, including a minimum of 3 years focused on oncology within biotech or pharma sectors. Experience with global early-stage oncology trials is essential, along with expertise in trial design, protocol development, and statistical analysis plan review. The role also demands strong communication skills and the ability to work flexible hours with teams across Europe and Asia, which may include travel requirements. In addition to technical expertise, the role necessitates building strong relationships with study sites, vendors, and internal stakeholders, ensuring compliance, ethics, and data integrity in trial conduct. The Medical Director will integrate new clinical insights into trial plans and collaborate closely with research leadership. The candidate will be involved in data monitoring activities and play a key role in clinical and scientific decision-making processes through comprehensive literature reviews. The client is committed to providing a supportive and ethical working environment, promoting equality, and offering opportunities for growth and development.