Clinical Development Medical Lead

Contenuto del lavoro

The CDMA will work very closely with R&D (including Clinical Operations), regulatory affairs, TA medical leads, and New Product Planning (NPP) team to ensure the successful local business development for future pipeline. The CDMA will also act as a peer scientific guide who communicates accurate and applicable scientific information to internal stakeholders and KEEs (key external experts) and collects relevant insight for pipeline portfolio.

In addition, the CDMA will own the local strategy for early external scientific engagement in the new therapeutic areas. He/she will identify key scientific experts, engage with them and maintain collegial and professional relationships. He/she will closely work to identify collaboration opportunities and ensure to collect actionable insights in new fields of engagement.

The CDMA will report directly to the Country Medical Director.

Typical Accountabilities:

• Co-lead NPP taskforce team
• Scientific Communication
• KEE Engagement & Development
• Develop and maintain the highest scientific and medical expertise in the relevant fields and be acknowledged internally and externally as an expert & resource in the assigned therapeutic area
• Identify and address relevant educational gaps and relay those to Global and Country Medical Affairs
• Ensure timely and informative scientific/medical exchanges with customers and internal partners, in accordance with compliance policies and with legal requirements
• Build/maintain communication and collaboration model with clinical operation teams.
• Support clinical study feasibility, drive identification of potential sites and investigators for clinical trials
• Develop in depth knowledge of the assigned therapeutic areas,
• Obtain valuable and actionable insights from the field to be shared with internal stakeholders
• Stay current of local laws and guidelines, codes of practices and AstraZeneca policies relevant to Clinical Development and Medical Affairs activity