Sumitomo Pharma
Director, Medical Affairs Strategy (Prostate Cancer)
Sumitomo Pharma, Providence, Rhode Island, us, 02912
Sumitomo Pharma Director, Medical Affairs Strategy (Prostate Cancer) Providence, Rhode Island Apply Now
Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the U.S., Canada, and Europe focused on addressing patient needs in oncology, urology, women's health, rare diseases, psychiatry & neurology, and cell & gene therapies. For more information on SMPA, visit our website
here
or follow us on
LinkedIn . Job Overview The
Director, Medical Strategy (Prostate Cancer)
will be a key member of the Medical Affairs team reporting to the Executive Director, Medical Affairs Strategy. This role is responsible for developing the strategic direction and alliance management for the Prostate Cancer therapeutic area, setting the strategy for both internal company programs and external facing interactions. Job Duties and Responsibilities Develops and aligns Medical Affairs strategic plans with brand strategic imperatives based on external engagement, MSL/cross functional input and impactful insights. Serves as a Medical Strategy lead for the Pfizer alliance for Prostate, ensuring coordination and alignment of all Medical Affairs activities and budget within SMPA and with alliance partners. Oversees the strategy and development of Medical Affairs plans and scientific platforms. Ensures cross-functional medical alignment with the US Field Medical team, Medical Communications & Operations, RWE & HEOR and ex-US colleagues. Directs the implementation of plans executed through multi-modal medical education channels, including publications, presentations, congresses, advisory boards, CME, and medical symposia. Oversees the development and implementation of detailed scientific Publication Plans. Works with cross functional teams to develop and execute Medical Advisory Board Plans. Engages externally and maintains a highly visible role within the medical/scientific community to develop relationships with scientific key opinion leaders. Collaborates with the commercial organization to align medical perspectives with commercial strategies. Partners with the Research & Development organization for ongoing and post-lifecycle team input. Defines and attends relevant medical and scientific conferences to support speakers, ensure success of publication goals, and report competitive intelligence. Provides input into Medical Education programs. Oversees the development of a supportive US Investigator Initiated Study and Collaborative Research program. Ensures medical review and approval of external resources, communications, and publications for accuracy and relevance. Develops and oversees Medical Affairs annual operating budget. Ensures compliance with corporate and healthcare guidance in all activities. Ability to travel (domestic and some international) to attend scientific congresses, participate in internal meetings, and meet key stakeholders - up to 30% travel. Key Core Competencies Strategic thinking and critical analysis. Ability to independently engage external stakeholders. Excellent verbal and written communication skills. Ability to effectively collaborate and deliver in a fast-paced environment. Strong interpersonal skills with experience in conflict management. Capability to analyze complex issues and develop realistic plans. One-Team attitude with cross-functional collaboration skills. Proven track record of medically accurate writing and review skills. Education and Experience Advanced degree in medical science (MD, PhD); MD with relevant specialization preferred. 8+ years of relevant Medical Affairs work experience in biotech or pharmaceutical industry, or equivalent professional clinical experience. The base salary range for this role is $225,200 to $281,500, including a comprehensive benefits package. Confidential Data : All information encountered is considered confidential. Compliance : Achieve and maintain compliance with all applicable regulatory and operational rules. Mental/Physical Requirements : Fast-paced environment handling multiple demands; requires excellent communication skills and the ability to use a personal computer for extended periods. Sumitomo Pharma America (SMPA) is an Equal Employment Opportunity (EEO) and Affirmative Action employer.
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Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the U.S., Canada, and Europe focused on addressing patient needs in oncology, urology, women's health, rare diseases, psychiatry & neurology, and cell & gene therapies. For more information on SMPA, visit our website
here
or follow us on
LinkedIn . Job Overview The
Director, Medical Strategy (Prostate Cancer)
will be a key member of the Medical Affairs team reporting to the Executive Director, Medical Affairs Strategy. This role is responsible for developing the strategic direction and alliance management for the Prostate Cancer therapeutic area, setting the strategy for both internal company programs and external facing interactions. Job Duties and Responsibilities Develops and aligns Medical Affairs strategic plans with brand strategic imperatives based on external engagement, MSL/cross functional input and impactful insights. Serves as a Medical Strategy lead for the Pfizer alliance for Prostate, ensuring coordination and alignment of all Medical Affairs activities and budget within SMPA and with alliance partners. Oversees the strategy and development of Medical Affairs plans and scientific platforms. Ensures cross-functional medical alignment with the US Field Medical team, Medical Communications & Operations, RWE & HEOR and ex-US colleagues. Directs the implementation of plans executed through multi-modal medical education channels, including publications, presentations, congresses, advisory boards, CME, and medical symposia. Oversees the development and implementation of detailed scientific Publication Plans. Works with cross functional teams to develop and execute Medical Advisory Board Plans. Engages externally and maintains a highly visible role within the medical/scientific community to develop relationships with scientific key opinion leaders. Collaborates with the commercial organization to align medical perspectives with commercial strategies. Partners with the Research & Development organization for ongoing and post-lifecycle team input. Defines and attends relevant medical and scientific conferences to support speakers, ensure success of publication goals, and report competitive intelligence. Provides input into Medical Education programs. Oversees the development of a supportive US Investigator Initiated Study and Collaborative Research program. Ensures medical review and approval of external resources, communications, and publications for accuracy and relevance. Develops and oversees Medical Affairs annual operating budget. Ensures compliance with corporate and healthcare guidance in all activities. Ability to travel (domestic and some international) to attend scientific congresses, participate in internal meetings, and meet key stakeholders - up to 30% travel. Key Core Competencies Strategic thinking and critical analysis. Ability to independently engage external stakeholders. Excellent verbal and written communication skills. Ability to effectively collaborate and deliver in a fast-paced environment. Strong interpersonal skills with experience in conflict management. Capability to analyze complex issues and develop realistic plans. One-Team attitude with cross-functional collaboration skills. Proven track record of medically accurate writing and review skills. Education and Experience Advanced degree in medical science (MD, PhD); MD with relevant specialization preferred. 8+ years of relevant Medical Affairs work experience in biotech or pharmaceutical industry, or equivalent professional clinical experience. The base salary range for this role is $225,200 to $281,500, including a comprehensive benefits package. Confidential Data : All information encountered is considered confidential. Compliance : Achieve and maintain compliance with all applicable regulatory and operational rules. Mental/Physical Requirements : Fast-paced environment handling multiple demands; requires excellent communication skills and the ability to use a personal computer for extended periods. Sumitomo Pharma America (SMPA) is an Equal Employment Opportunity (EEO) and Affirmative Action employer.
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