About the role:
- RLT MLL serves as an ambassador and an advocate for AAA science withinthe healthcare community, and works directly with Nuclearmedicine/oncology healthcare professionals across accounts, educatestargeted radioligand treatment centers about appropriate setup, process,handling, administration and infrastructure, and as well as to discussand provide scientific and therapeutic information on appropriateradiopharmaceutical licensing for Lu177, Ga 68 and other relevant radio linkers
- In line with overall product strategy, the RLT MLL is responsible forsupporting regional strategy, implementation and execution of MedicalAffairs plans for radioligand therapy and radioligand imaging, providingscientific information, helping design and organize clinical studies,building educational dialogue with KOLs and regulatory stakeholders
- Provide regional RLT leadership to accelerate the registration for new pipeline
Key Responsibilities:
•Be a strategic internal partner, gather and leverage insights for animpactful contribution to Patient Journey mapping, launch excellenceroadmap, integrated evidence generation plans, integrated productstrategy and subsequently the medical strategy.
•Utilize knowledge of assigned therapeutic area and Novartis compoundsto serve as the Medical, Clinical and Scientific expert to field matrix colleagues
•Ensure appropriate identification and mapping of external stakeholders,aligned to the medical strategy, and in collaboration with otherNovartis colleagues. Able to create personalized, flexible engagementstrategies and plans, leveraging multiple channels and tailored contentto meet the changing needs of external stakeholders
•Respond to unsolicited requests for information from stakeholders bysharing appropriate data regarding marketed and pipeline compounds in atimely, compliant, and stakeholder-focused manner.
•Manage administrative responsibilities in a timely manner (customerrelationship management tool, compliance training and other modules,expense reporting, etc.).
•Promote and adhere to Ethics and Compliance Professional PracticesPolicy (P3).
•Reporting of technical complaints / adverse events / special casescenarios related to Novartis products within 24 hours of receipt.Distribution of marketing samples
Essential Requirements:
•MD, PharmD., pharmacist, PhD, Master above degree in medical or otherlife sciences
•Ability of Chinese and English
•Medical Science and Disease Area Knowledge
•Strategic& Enterprise Mindset
•Stakeholder Engagement& Experience
•Healthcare systems& partnerships
•Joint Value Creation& Collaboration
Why Novartis: Helping people with disease and their families takes morethan innovative science. It takes a community of smart, passionatepeople like you. Collaborating, supporting and inspiring each other.Combining to achieve breakthroughs that change patients’ lives.