Opportunity Details

The client is seeking a Temporary Clinical Science Director located in Pennsylvania or New Jersey to collaborate with clinical and project teams in designing and developing studies in early and/or late phase clinical oncology. Responsibilities include preparing study synopses, protocols, and summarizing study results for documents and publications. The director will interact with investigators and thought leaders in oncology, conduct literature research, and collaborate with internal team members to develop study materials. Additionally, they will participate in safety meetings, analyze potential safety events, and contribute to regulatory filing documentation.

The ideal candidate will have a Pharm.D., PhD, or M.D. with a minimum of 8 years of related experience in clinical development in the biotechnology or pharmaceutical industry. They should have 5-8 years of experience in clinical oncology studies with molecular targeted or immunological therapies. Strong knowledge of clinical trial implementation, drug development processes, and experience in designing, executing, and reporting clinical trials in oncology is required. The director must be able to lead and manage teams, provide guidance based on organizational goals, and have strong analytical and communication skills.

Overall, the Temporary Clinical Science Director will play a key role in coordinating and facilitating clinical oncology studies, maintaining relationships with study investigators, delivering scientific presentations to external customers, and providing clinical education support internally. This position requires up to 25% travel and offers the opportunity to contribute to the development of investigational agents, abstracts, publications, and presentations for scientific meetings. The director will stay current on emerging clinical and competitive trends in the field of Oncology and maintain clinical and technical expertise in the therapeutic area.