Daiichi Sankyo US
Overview
The Director US Medical Affairs (USMA) Oncology, under the direction of the Senior Director, USMA Oncology (US 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. The role is primarily responsible for US Medical Affairs Strategy and overseeing execution of medical activities for assigned indication(s) and asset(s) and will have the responsibility of managing multiple direct reports.
Responsibilities
Leads the development of the US Medical Affairs strategy and execution of the US 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 medical affairs plan activities, in collaboration with Sr. Director.
Leads medical readiness activities for market launches. This includes strategic partnerships with the brand team, HEOR, RD, FMA, MIE and global functions as necessary to create and implement strategies that support launch. Provide medical support/input into commercial and market access discussions for select indications.
Provides medical leadership in interactions with key external stakeholders including scientific leaders, payers and societies; 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.
Responsible for scientific communications and publications; interpretation of clinical data; ensuring consistency of clinical content and scientific statements across materials; training or communication of emerging data (internal or competitive), such as congress updates and development program highlights; and budget and forecast accuracy.
In a matrix environment, represents US interests and business needs in shaping development and life cycle management strategy for select indications/projects. Reviews Externally Sponsored Research (ESRs) and may serve as deputy regional medical lead in Global IIS Review Committee meetings. May serve as medical lead for select company-sponsored evidence generating studies/projects. Manages all medical aspects such as study document development and drives execution for assigned projects in collaboration with USMA Clinical Operations and other cross-functional and regional stakeholders.
Qualifications Education Qualifications (from an Accredited College Or University)
An advanced doctorate degree (PharmD, Ph.D., MD, DO, or equivalent) in a medical/ scientific area is required. Experience in oncology therapeutic area is required
Experience Qualifications
10 or More Years overall related experience or commensurate education/experience required
4 or More Years experience in pharma at local, regional and/or Global level. preferred
Excellent knowledge of current clinical practice in Oncology / Hematology or other relevant disease area. preferred
knowledge in and understanding of medical activities (including scientific communications, medical information, MSLs, and HEOR), relating to the commercialization of oncology products preferred
Travel: Up to 20% travel; standard office-based physical demands, travel as required.
Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.
Salary Range
$198,160.00 - $297,240.00
Seniority level
Not Applicable
Employment type
Full-time
Job function
Health Care Provider
Industries
Biotechnology Research
Hospitals and Health Care
Pharmaceutical Manufacturing
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Responsibilities
Leads the development of the US Medical Affairs strategy and execution of the US 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 medical affairs plan activities, in collaboration with Sr. Director.
Leads medical readiness activities for market launches. This includes strategic partnerships with the brand team, HEOR, RD, FMA, MIE and global functions as necessary to create and implement strategies that support launch. Provide medical support/input into commercial and market access discussions for select indications.
Provides medical leadership in interactions with key external stakeholders including scientific leaders, payers and societies; 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.
Responsible for scientific communications and publications; interpretation of clinical data; ensuring consistency of clinical content and scientific statements across materials; training or communication of emerging data (internal or competitive), such as congress updates and development program highlights; and budget and forecast accuracy.
In a matrix environment, represents US interests and business needs in shaping development and life cycle management strategy for select indications/projects. Reviews Externally Sponsored Research (ESRs) and may serve as deputy regional medical lead in Global IIS Review Committee meetings. May serve as medical lead for select company-sponsored evidence generating studies/projects. Manages all medical aspects such as study document development and drives execution for assigned projects in collaboration with USMA Clinical Operations and other cross-functional and regional stakeholders.
Qualifications Education Qualifications (from an Accredited College Or University)
An advanced doctorate degree (PharmD, Ph.D., MD, DO, or equivalent) in a medical/ scientific area is required. Experience in oncology therapeutic area is required
Experience Qualifications
10 or More Years overall related experience or commensurate education/experience required
4 or More Years experience in pharma at local, regional and/or Global level. preferred
Excellent knowledge of current clinical practice in Oncology / Hematology or other relevant disease area. preferred
knowledge in and understanding of medical activities (including scientific communications, medical information, MSLs, and HEOR), relating to the commercialization of oncology products preferred
Travel: Up to 20% travel; standard office-based physical demands, travel as required.
Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.
Salary Range
$198,160.00 - $297,240.00
Seniority level
Not Applicable
Employment type
Full-time
Job function
Health Care Provider
Industries
Biotechnology Research
Hospitals and Health Care
Pharmaceutical Manufacturing
#J-18808-Ljbffr