摘要
~設計中およびプログラムのエンドツーエンドの実行に沿って、医学的/科学的/証拠生成のインプットを提供します。
~統合エビデンス計画(IEP)/機能別プログラムの開発と実行にインプットを提供し、優先的な上市ポートフォリオの価値提案と医薬品の影響を最大化します。
About the Role
Role Purpose:
The Lead, TA Medical or Associate, TA Medical is accountable for building responsible brand
or disease area medical strategy and ensuring its execution in collaboration with MSLs, MSEs
and other partners with support from Head, TA Medical, Senior leads, TA Medical and/or Leads,
TA Medical. The Lead, TA Medical or Associate, TA Medical is the key project representative
to commercial and GDD within Japan, and to global medical outside of Japan.
Four TAs – Haematology, Solid Tumour, Speciality Medicine and General Medicine.
Major Accountabilities
The Lead, TA Medical or Associate, TA Medical is accountable for all of the below items with
support from Head, TA Medical, Senior leads, TA Medical and/or Leads, TA Medical.
• Bring clarity to the medical strategy and the tactics in the therapeutic area by their own
medical/scientific knowledge/interpretation/judgement and deep understanding of external
voice/environment as medical/scientific/clinical research expert.
o Develop outcome-focusing TA Medical strategy aligned with TA strategy from
both local and global points of view
o Act as “Medical lead” in the agile project
o Drive the actionable insight cycle by giving regular clear direction to MSLs on
activities, messaging, targets, etc., and utilize collected insights to further refine the
medical tactics
o Work with PMO to shape the project work breakdown structure for the TA and to
identify/secure required resources and budget of the teams
o Input local needs into global strategy and collaborate with global teams on global
project
o Develop omnichannel engagement (OCE) plan by conducting omnichannel data
analysis in collaboration with OCE capability pool and Medical Science group
• Lead/execute the evidence generation strategy in the responsible therapeutic areas as a
medical/scientific/clinical research expert through scientific publications and innovative
medical solutions in close collaboration with internal and external stakeholders.
o Plan/lead/execute primary data collection (PDC) and secondary use data (SUD)
studies including retrospective researches, prospective researches, biomarker
researches, translational researches, database studies, etc. in collaboration with
ME&E Dept.
o Plan/execute Integrated Evidence generation Plan (IEP) by leading cross functional
team
• Provide training for the organization he/she belongs to by leveraging highly advanced
medical/scientific/clinical research expertise in the therapeutic area.
• Work as Patient Engagement Liaison (PEL).
Background
Education:
• Master’s degree or equivalent experiences. Advanced science degree
(MD, PhD, PharmD, MPH etc) strongly preferred
Languages:
• Japanese, Intermediary English
Experience/Professio
nal requirement:
• At Least 3-year agile project management not in a software
development but in a business context
• Preferred (not essential): Knowledge of healthcare industry
• 3-year experience corresponding to MSE/SciComm or
Marketing/JPH/JPCH
Competency • Agile Project Management
• Strategic and logical thinking skill
• Scientific hypothesis construction skill
• Communication skill with external specialists
• Research publication skill
• Deep knowledge of TA
• Ability to synthesize complex requirements into clear specifications
• Strong relationship management and natural collaborator
• Cost Management skills
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture
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