Medical Advisor (Oncology)

Medical Advisor (Oncology)
The Medical Advisor is responsible for the development and registration clinical trials (from Phase II to Phase III), providing thorough up-to-date relevant medical expertise to contribute to Novartis development and registration strategies and collaborating with local and Global teams.

Major Acountabilities:
1. Strategic: Development and registration of assigned new OGD (Oncology Global Development) and OTM (Oncology Traslational Medicine) compounds
2. Operational: contribute and provide support to the local GMO (Global Monitoring Operations) team for implementation and timely execution of studies conducted in the Country and to DRA (Drug Regulatory Affairs) in interactions with Ethical Review Boards (ERBs) and Health Authorities (HAs).
3. Collaborate effectively with Country, Region Europe and Global Development teams in the execution of relevant clinical activities, including initial inputs and provide contribution to handle advisory boards
4. May serve as local representative on Global teams.
5. Contribute with medical and clinical expertise to finalization of OGD/OTM Strategies, GDBS (Global Development Plans Strategy), CDBS (Clinical Development Plans) and Study Protocols; provide scientific advice to all allied departments in local CPO.
6. May work as strategic partner with Medical Affairs and Marketing for assigned compound(s) within the CPO teams.
University Degree in Medicine (Oncology field is a plus)
Fluent English (oral and written).
Experience of 3 to 5 years in clinical medicine and/or research;
Previous experience in Oncology and Melanoma is highly preferred
Novartis Farma IT
Research & Development
Full Time