• Support Clinical Development in Prostate cancer • Supporting the development, execution and communication of the global scientific/medical evidence plan • Supporting cross-functional and global collaborations to integrate broad medical, scientific, and commercial input into the development program • Supporting the development of key scientific external relationships with opinion leaders • Participating and providing clinical input into safety and regulatory interactions • Provide clinical/scientific input during the development and execution of clinical trials • Interpret clinical trial data • Participate in safety assessments • Participate in interactions with regulatory agencies • Author CSRs, publications and regulatory submissions • Develop key opinion leaders and make scientific presentation at advisory boards, key scientific meetings and external committee meetings as delegated by Global Development Leader • Identify new clinical research opportunities • Support in-licensing and out-licensing activities and partner relationships • Support product lifecycle management for new indications as directed by Global Development Leader • Provide clinical content input to: Regulatory interactions and documents; Safety interactions and documents; Materials to be used in Scientific Affairs; Materials to be used by the Commercial Organization