Director, Global Leadership Development - Îles Éparses, France - Daiichi Sankyo

Description

Director Global Medical Affairs Oncology (GMA) (m/f/x)

in oncology our goal is to become a global pharma innovator until 2025 by providing novel therapies to patients across the world.

Director Global Medical Affairs Oncology (GMA) (m/f/x)

The Director Global Medical Affairs Oncology (GMA) (m/f/x), ADC, under the direction of the Senior Director, GMA Oncology ADC (Global Medical Affairs team lead for compound), is responsible for assisting with defining compound/program medical strategies and for leading select medical affairs projects within a specific compound or indication.

Leads the development of the Global Medical Affairs strategy and execution of the Global Medical Affairs plan for select indications/projects related to evidence generation, medical information and internal education, publications, scientific exchange and external data communication, and stakeholder scientific engagement.

Responsible for managing budgets and resources for the assigned GMA plan activities, in collaboration with Sr Director.
Leads medical readiness activities for market launches and life cycle management for select indications/projects.

Gains strategic and planning alignment across regions and functions and supports review of Local Country/Regional Medical Affairs activities when applicable.

Serve as medical lead for select company-sponsored GMA evidence generating studies/projects.

Manages all medical aspects such as study document development and drives execution for assigned projects in collaboration with GMA Clinical Operations and other cross-functional and regional stakeholders.

Leads external medical education and other scientific exchange activities in alignment with the Senior Director, such as scientific symposium and medical congresses, within legal and compliance regulations.

Collaborates across functions to support GMA MI&E activities in order to achieve approval of key scientific communications resources such as medical information response documents, (non-) promotional materials, educational slide deck and other internal training resources, within legal and compliance regulations.

Provides medical leadership in interactions with key external stakeholders and lead Scientific Engagement activities such as planning advisory boards, managing individual stakeholder interactions and peer to peer discussions, congress engagement activities, and collation of insights for select indications related to the compound.

An advanced doctorate degree (PharmD, PhD, MD, DO or equivalent) in medical/ scientific area is required. Effectively manages activities and optimize resources and budget to meet business needs; have excellent project management skills
Conduct medical/legal review
Effectively engage external stakeholders across a broad range of audiences and activities such as evidence generation projects, publications, medical information and education, Advisory Boards, Scientific Exchange)
Expertly manage ambiguity and highly complex situations
Internal Project and Budget Accountability
Fluent English (oral and written)