Clinical Development Director, Chronic Weight Management

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.