The Nephrology Therapeutic Area is looking for a Clinical Research Medical Director who will be responsible for:
- 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.
Key activities include the following:
- 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 publications and regulatory submissions
- Develop key opinion leaders and make scientific presentation at advisory boards key scientific meetings and external committee meetings.
- 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
Clinical input into the following:
- Regulatory interactions and documents
- Safety interactions and documents
- Materials to be used in Scientific Affairs
- Materials to be used by the Commercial Organization
