Sumitomo Pharma
Director, Medical Affairs Strategy (Hematology/Oncology)
Sumitomo Pharma, Columbia, South Carolina, us, 29228
Sumitomo Pharma Director, Medical Affairs Strategy (Hematology/Oncology) Columbia, South Carolina 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 Overview The Director, Medical Affairs Strategy (Hematology/Oncology) will be a key member of the Medical Affairs team reporting to the Executive Director, Medical Affairs Strategy. In this role, individuals are responsible for Medical Affairs strategic direction and management for Pipeline Hematology/Oncology asset(s), leading the Medical Affair planning for both internal company programs and external facing interactions. The job will oversee the management peri-, pre-, and post-launch activities related to Medical Affairs function. This individual will lead program coordination with Clinical Development leadership to ensure alignment between Medical Affairs, Advocacy, Translational Medicine, and Commercial launch strategy and guide the tactical implementation of Medical Affairs plans. Job Duties and Responsibilities Ensure leadership and alignment of all Medical Affairs activities and budgets for Pipeline Hematology/Oncology Product(s) within SMPA. Manage the development of Medical Affairs strategic plans and scientific platforms in support of Pipeline Hematology/Oncology Product(s). Represent the Oncology Products Medical Strategy Team within the Medical Affairs leadership and executive leadership teams. Serve as Subject Matter Expert within Medical Affairs Team provide medical training, evaluation, motivation, and control of activities in alignment with the company’s corporate strategies and objectives. Lead cross-functional medical alignment with the US Field Medical team, Medical Communications & Operations, Japan medical affairs colleagues, RWE (Real World Evidence) & HEOR (Health Economics and Outcomes Research). Develop and direct the implementation of plans that will be executed through multi-modal medical education channels. Manage the development and implementation of detailed scientific Publication Plans, Medical Advisory Boards, and Patient Advisory Boards. Represent the Medical Affairs department on the lifecycle team to provide medical affairs input to Clinical Development and Clinical Operation’s needs. Proactively seek and create relationships directly with key opinion leaders, prominent clinical investigators, and scientific advisory groups. Work closely with the commercial organization to bring the medical and pharmacoeconomic perspectives to commercial strategies and tactics. Partner with the Clinical Development organization for ongoing and post-marketing clinical development activities. Provide detailed and compliant medical review and approval of external resources, communications, and publications. Define and attend relevant medical and scientific conferences to help coordinate medical affairs activities. Provide input into budget and long-term Medical Education programming or Medical Sponsorships. Ensure that all interactions and activities in the US adhere to corporate and healthcare compliance guidance. Serves as Medical Affairs Lead on select therapeutics topics, and provides input into developing scientific messages. Provide feedback on Medical Information response documents. Ability to travel (domestic and some international) to attend scientific congresses, participate in internal meetings, and meet key stakeholders in the development of medical activities - up to 30% travel. Key Core Competencies Excellent verbal and written communication skills. Ability to effectively communicate, collaborate and deliver excellent work in a fast-paced environment. 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. Mentorship attitude with the capability to work cross-functionally. Capable of translating broad corporate objectives into actionable medical and scientific strategies. Proven record of accomplishment of detailed, medically accurate, and scientifically relevant writing and review skills. Experience representing a broad range of stakeholders in the development and communication of medical activities and plans. Education and Experience Advanced degree in medical science (MD, PharmD, PhD) or equivalent professional hematology/oncology clinical experience; with knowledge of the acute myeloid leukemia (AML) landscape is required. 8-10+ years of relevant professional experience in biotech, pharmaceutical industry, or related healthcare experience. Medical Affairs and strategic planning experience within a matrix team environment is considered a plus. Strong organizational skills, and familiarity working on PCs and the Microsoft Office Suite. Salary and Benefits The base salary range for this role is $187,800 to $234,700. Base salary is part of our total rewards package which also includes the opportunity for merit-based salary increases, short incentive plan participation, eligibility for our 401(k) plan, medical, dental, vision, life and disability insurances and leaves provided in line with your work state. Equal Employment Opportunity Sumitomo Pharma America (SMPA) is an Equal Employment Opportunity (EEO) and Affirmative Action employer. Sumitomo Pharma America (SMPA) is committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability, veteran or military status or liability for military status.
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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 Overview The Director, Medical Affairs Strategy (Hematology/Oncology) will be a key member of the Medical Affairs team reporting to the Executive Director, Medical Affairs Strategy. In this role, individuals are responsible for Medical Affairs strategic direction and management for Pipeline Hematology/Oncology asset(s), leading the Medical Affair planning for both internal company programs and external facing interactions. The job will oversee the management peri-, pre-, and post-launch activities related to Medical Affairs function. This individual will lead program coordination with Clinical Development leadership to ensure alignment between Medical Affairs, Advocacy, Translational Medicine, and Commercial launch strategy and guide the tactical implementation of Medical Affairs plans. Job Duties and Responsibilities Ensure leadership and alignment of all Medical Affairs activities and budgets for Pipeline Hematology/Oncology Product(s) within SMPA. Manage the development of Medical Affairs strategic plans and scientific platforms in support of Pipeline Hematology/Oncology Product(s). Represent the Oncology Products Medical Strategy Team within the Medical Affairs leadership and executive leadership teams. Serve as Subject Matter Expert within Medical Affairs Team provide medical training, evaluation, motivation, and control of activities in alignment with the company’s corporate strategies and objectives. Lead cross-functional medical alignment with the US Field Medical team, Medical Communications & Operations, Japan medical affairs colleagues, RWE (Real World Evidence) & HEOR (Health Economics and Outcomes Research). Develop and direct the implementation of plans that will be executed through multi-modal medical education channels. Manage the development and implementation of detailed scientific Publication Plans, Medical Advisory Boards, and Patient Advisory Boards. Represent the Medical Affairs department on the lifecycle team to provide medical affairs input to Clinical Development and Clinical Operation’s needs. Proactively seek and create relationships directly with key opinion leaders, prominent clinical investigators, and scientific advisory groups. Work closely with the commercial organization to bring the medical and pharmacoeconomic perspectives to commercial strategies and tactics. Partner with the Clinical Development organization for ongoing and post-marketing clinical development activities. Provide detailed and compliant medical review and approval of external resources, communications, and publications. Define and attend relevant medical and scientific conferences to help coordinate medical affairs activities. Provide input into budget and long-term Medical Education programming or Medical Sponsorships. Ensure that all interactions and activities in the US adhere to corporate and healthcare compliance guidance. Serves as Medical Affairs Lead on select therapeutics topics, and provides input into developing scientific messages. Provide feedback on Medical Information response documents. Ability to travel (domestic and some international) to attend scientific congresses, participate in internal meetings, and meet key stakeholders in the development of medical activities - up to 30% travel. Key Core Competencies Excellent verbal and written communication skills. Ability to effectively communicate, collaborate and deliver excellent work in a fast-paced environment. 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. Mentorship attitude with the capability to work cross-functionally. Capable of translating broad corporate objectives into actionable medical and scientific strategies. Proven record of accomplishment of detailed, medically accurate, and scientifically relevant writing and review skills. Experience representing a broad range of stakeholders in the development and communication of medical activities and plans. Education and Experience Advanced degree in medical science (MD, PharmD, PhD) or equivalent professional hematology/oncology clinical experience; with knowledge of the acute myeloid leukemia (AML) landscape is required. 8-10+ years of relevant professional experience in biotech, pharmaceutical industry, or related healthcare experience. Medical Affairs and strategic planning experience within a matrix team environment is considered a plus. Strong organizational skills, and familiarity working on PCs and the Microsoft Office Suite. Salary and Benefits The base salary range for this role is $187,800 to $234,700. Base salary is part of our total rewards package which also includes the opportunity for merit-based salary increases, short incentive plan participation, eligibility for our 401(k) plan, medical, dental, vision, life and disability insurances and leaves provided in line with your work state. Equal Employment Opportunity Sumitomo Pharma America (SMPA) is an Equal Employment Opportunity (EEO) and Affirmative Action employer. Sumitomo Pharma America (SMPA) is committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability, veteran or military status or liability for military status.
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