The organization is looking for a highly skilled clinical development physician to join as the Director of Clinical Oncology Programs, focusing on early-stage oncology trials. In this pivotal role, you will author clinical protocols and essential regulatory documents, such as clinical study reports and training materials. Your key responsibilities will encompass:
• Conducting thorough medical and safety/efficacy data reviews.
• Preparing comprehensive trial result summaries for diverse stakeholders.
• Managing drug safety activities effectively.
• Supporting clinical site initiation visits.

This position requires a profound understanding of oncology, strong clinical judgment, and the ability to collaborate effectively with global teams and external partners. Ideal candidates will hold an MD, MD/PhD, or an equivalent advanced clinical degree, paired with at least 5 years of clinical development experience in the industry, including a minimum of 3 years concentrated on oncology within the biotech or pharmaceutical sectors.

Experience with global early-stage oncology trials is crucial, along with proficiency in trial design, protocol development, and the review of statistical analysis plans. Excellent communication skills are essential, as is the flexibility to work with teams across Europe and Asia, which may include travel. Building robust relationships with study sites, vendors, and internal stakeholders is vital to ensuring compliance, ethics, and data integrity throughout trial conduct.

As the Director, you will integrate new clinical insights into trial plans, working closely with research leadership. You will participate in data monitoring activities and play a significant role in the clinical and scientific decision-making process through thorough literature reviews. We are committed to providing a supportive and ethical work environment that promotes equality and fosters your opportunities for growth and development.