Medical Oncology Head

• Adapt international medical plans into a

supporting prelaunch, launch and lifecycle management.

• Build a strategic orientation and

across external insights, medical education, and publication planning.

• Set and oversee the

(RWE, HEOR inputs, evidence generation, Phase IV/IIIb) including publication plans.

• Provide

to inform trial design, feasibility, integrated evidence strategies, and local clinical programs.

• Serve as the

for internal stakeholders (Marketing, Market Access, Regulatory, Commercial, Digital).

• Guarantee

• Lead and guide all

with HCPs and Medical Experts (MEs) to ensure credible, unbiased, scientific dialogue.

• Oversee MSL strategic direction, ensuring coherent field engagement plans aligned to TA strategy.
• Ensure systematic

and translate insights into strategic recommendations.

• Support internal teams with

, clinical data interpretation, and training.

• Ensure medical teams maintain highest standards in

.

Medical Education & Scientific Communication

• Design and execute the

, including scientific events, symposia, hospital meetings, and congress activities.

• Localize and produce high quality

(presentations, publications, external education tools).

• Partner with Medical Customer Excellence and other internal functions on

, vendor management, congress measurement and reporting.

• Lead or support publication planning for the country TA.

•

• Build and maintain strong

to support collaboration and scientific leadership in the TA.

• Partner cross-functionally with Commercial TA Heads, Value & Access, Regulatory, Execution Excellence and global/international/regional medical teams.
• Represent the company as the

in the TA, contributing to a positive reputation with key stakeholders and institutions.

• Strengthen the medical ecosystem by shaping

• Foster an engaged, high-performance culture with clear goals, coaching, and ongoing development.
• Attract future ready talents, help them grow, and keep them engaged; strengthen succession and capability across the country organization.
• Lead by example with Novartis Leadership Expectations, encouraging transformation, strong performance, and a growth mindset.

• 7+ years in Medical Affairs and/or Clinical Development
• Experience working in Oncology Therapeutic Area
• Proven track record in developing and executing

across the product lifecycle.

• Prior

• Experience in

with Medical Experts/HCPs and guiding MSL/field medical teams.

• Demonstrated experience in

, publication planning, and interpreting clinical data.

• Cross‑functional collaboration experience with

.

• Experience leading

, congress activities, and external scientific events.

• Exposure to regional/global medical functions with ability to translate strategy into local action.
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• Ability to design and deliver

, translating global direction into local execution.

• Strong scientific expertise with ability to

.

• Skilled in planning and overseeing

(RWE, Phase IV, observational research).

• Proficient in developing/adapting

.

• Strong

• Ability to collaborate effectively across matrix teams and provide clear

to cross‑functional partners.

• Solid understanding of

regulatory requirements, and governance processes.

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• Strategic thinker who can anticipate trends and translate insights into clear

.

• Influential leader able to

and build trust with internal/external partners.

• Strong people leader who develops others through coaching, feedback, and scientific role modeling.
• Drives execution and fosters a

, evidence-based culture.

• Comfortable navigating

while driving innovation and continuous improvement.

• Excellent communicator with the ability to simplify complex scientific concepts for diverse audiences.
• High integrity, ethical judgment, and a patient centric mindset guiding all interactions.