Sumitomo Pharma
Director, Medical Affairs Strategy (Women's Health)
Sumitomo Pharma, Boise, Idaho, United States, 83708
Sumitomo Pharma Director, Medical Affairs Strategy (Women's Health) Boise, Idaho Apply Now
Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the U.S. (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma Canada, Inc.) and Europe (Sumitomo Pharma Switzerland GmbH) focused on addressing patient needs in oncology, urology, women's health, rare diseases, psychiatry & neurology, and cell & gene therapies.Job OverviewThe Director, Medical Strategy (Women’s Health) will be a key member of the Medical Affairs team reporting to the Executive Director, Medical Affairs Strategy.This job is responsible for strategic direction and alliance management for the Women’s Health (WH) therapeutic area and sets strategy for both internal company programs and external facing interactions. This job will effectively lead and communicate with cross-functional team members to share and gain insights that help SMPA meet the unmet medical needs in Women’s Health – Endometriosis and Uterine Fibroids.Job Duties and ResponsibilitiesDevelops and aligns Medical Affairs strategic plans with brand strategic imperatives that support impactful insights, data generation, and data communication plans to support education and awareness to HCP stakeholders and healthcare payers.Serve as a Medical Strategy lead for the Pfizer alliance for Women’s Health, ensuring coordination and alignment of all women’s health Medical Affairs activities and budget within SMPA and with alliance partners.Oversee the strategy and development of Medical Affairs plans and scientific platforms for relugolix combination therapy.Develop the Medical Strategy Team within the US to provide medical training, evaluation, motivation, and control of activities in alignment with the company’s corporate strategies and objectives.Ensure cross-functional medical alignment with the US Field Medical team, Medical Communications & Operations, RWE & HEOR and ex-US colleagues.Direct the implementation of plans that will be executed through multi-modal medical education channels, including publications, presentations, congresses, advisory boards, CME, medical symposia and other channels in support of relugolix combination therapy commercialization.Oversee the development and implementation of detailed scientific Publication Plans & Medical Advisory Board Plan.Play a highly visible role during exchanges within the medical/scientific community to develop close relationships with a group of scientific key opinion leaders.Work closely with the commercial organization to bring the medical perspective to commercial strategies and tactics.Partner with the Research & Development organization for ongoing and post-Represent the Medical Affairs department on the lifecycle team for WH to provide Medical Affairs input to R&D.Define and attend relevant medical and scientific conferences to support speakers and presenters, ensure the success of publication/communication goals, and participate in the collection and reporting of competitive intelligence within company guidelines.Provide strategy and oversight for the development of a supportive US Investigator Initiated Study program.Provide detailed and compliant medical review and approval of external resources, communications, and publications – ensuring medical accuracy, relevance, and fair-balance.Develops and oversees Medical Affairs annual operating budget.Ensures that all interactions and activities in the US adhere to corporate and healthcare compliance guidance.Ability to travel (domestic and some international) to attend scientific congresses, participate in internal meetings, and meet key stakeholders in the development of Medical Affairs activities - up to 25% travel.Key Core CompetenciesExcellent verbal and written communication skills, as the position will interface with key opinion leaders and a wide range of internal employees.Ability to effectively communicate, collaborate and deliver excellent work in a fast-paced, and rapidly changing dynamic company.Must have excellent interpersonal skills, with experience in conflict management and relationship building.Ability to analyze complex issues critically and develop realistic and accomplishable plans and solutions.One-Team attitude with the capability to work cross-functionally with peers and other colleagues.Capable of translating brand goals and objectives into actionable medical and scientific strategies.Proven track record of detailed, medically accurate, and scientifically relevant writing and review skills in line with compliance requirements.Experience representing a broad range of stakeholders in the development and communication of medical activities and plans.Education and ExperienceAdvanced degree in medical science (MD, PharmD, PhD); MD with relevant specialization preferred.8+ years of relevant Medical Affairs work experience in biotech or pharmaceutical industry, or equivalent professional clinical experience in the field of WH medicine.Experience leading in a matrix team environment is considered a plus.Strong computer skills (Microsoft Office, etc.), knowledge of database management (Veeva Vault, etc.), and other enterprise platforms required for business.
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Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the U.S. (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma Canada, Inc.) and Europe (Sumitomo Pharma Switzerland GmbH) focused on addressing patient needs in oncology, urology, women's health, rare diseases, psychiatry & neurology, and cell & gene therapies.Job OverviewThe Director, Medical Strategy (Women’s Health) will be a key member of the Medical Affairs team reporting to the Executive Director, Medical Affairs Strategy.This job is responsible for strategic direction and alliance management for the Women’s Health (WH) therapeutic area and sets strategy for both internal company programs and external facing interactions. This job will effectively lead and communicate with cross-functional team members to share and gain insights that help SMPA meet the unmet medical needs in Women’s Health – Endometriosis and Uterine Fibroids.Job Duties and ResponsibilitiesDevelops and aligns Medical Affairs strategic plans with brand strategic imperatives that support impactful insights, data generation, and data communication plans to support education and awareness to HCP stakeholders and healthcare payers.Serve as a Medical Strategy lead for the Pfizer alliance for Women’s Health, ensuring coordination and alignment of all women’s health Medical Affairs activities and budget within SMPA and with alliance partners.Oversee the strategy and development of Medical Affairs plans and scientific platforms for relugolix combination therapy.Develop the Medical Strategy Team within the US to provide medical training, evaluation, motivation, and control of activities in alignment with the company’s corporate strategies and objectives.Ensure cross-functional medical alignment with the US Field Medical team, Medical Communications & Operations, RWE & HEOR and ex-US colleagues.Direct the implementation of plans that will be executed through multi-modal medical education channels, including publications, presentations, congresses, advisory boards, CME, medical symposia and other channels in support of relugolix combination therapy commercialization.Oversee the development and implementation of detailed scientific Publication Plans & Medical Advisory Board Plan.Play a highly visible role during exchanges within the medical/scientific community to develop close relationships with a group of scientific key opinion leaders.Work closely with the commercial organization to bring the medical perspective to commercial strategies and tactics.Partner with the Research & Development organization for ongoing and post-Represent the Medical Affairs department on the lifecycle team for WH to provide Medical Affairs input to R&D.Define and attend relevant medical and scientific conferences to support speakers and presenters, ensure the success of publication/communication goals, and participate in the collection and reporting of competitive intelligence within company guidelines.Provide strategy and oversight for the development of a supportive US Investigator Initiated Study program.Provide detailed and compliant medical review and approval of external resources, communications, and publications – ensuring medical accuracy, relevance, and fair-balance.Develops and oversees Medical Affairs annual operating budget.Ensures that all interactions and activities in the US adhere to corporate and healthcare compliance guidance.Ability to travel (domestic and some international) to attend scientific congresses, participate in internal meetings, and meet key stakeholders in the development of Medical Affairs activities - up to 25% travel.Key Core CompetenciesExcellent verbal and written communication skills, as the position will interface with key opinion leaders and a wide range of internal employees.Ability to effectively communicate, collaborate and deliver excellent work in a fast-paced, and rapidly changing dynamic company.Must have excellent interpersonal skills, with experience in conflict management and relationship building.Ability to analyze complex issues critically and develop realistic and accomplishable plans and solutions.One-Team attitude with the capability to work cross-functionally with peers and other colleagues.Capable of translating brand goals and objectives into actionable medical and scientific strategies.Proven track record of detailed, medically accurate, and scientifically relevant writing and review skills in line with compliance requirements.Experience representing a broad range of stakeholders in the development and communication of medical activities and plans.Education and ExperienceAdvanced degree in medical science (MD, PharmD, PhD); MD with relevant specialization preferred.8+ years of relevant Medical Affairs work experience in biotech or pharmaceutical industry, or equivalent professional clinical experience in the field of WH medicine.Experience leading in a matrix team environment is considered a plus.Strong computer skills (Microsoft Office, etc.), knowledge of database management (Veeva Vault, etc.), and other enterprise platforms required for business.
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