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US-Remote

Full time

R01579

Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc.), focused on addressing patient needs in oncology, urology, women's health, rare diseases, cell & gene therapies and CNS. With several marketed products and a diverse pipeline of early- to late-stage investigational assets, we aim to accelerate discovery, research, and development to bring novel therapies to patients sooner. For more information on SMPA, visit our website https://www.us.sumitomo-pharma.com or follow us on LinkedIn.

Job Overview

The Associate Director, Medical Strategy (Prostate Cancer) will be a key member of the Medical Affairs team and will report to the Medical Affairs Director, Solid Tumors TA Lead. The position will serve as the Associate Director for assigned prostate cancer projects, providing medical and scientific leadership and partnering with the TA Lead to develop and execute Medical Affairs strategy for internal programs and external-facing interactions. The role will work in close, ongoing partnership with the TA Lead, with regular alignment on priorities, strategic direction, execution, and escalation of key issues. This position will lead and communicate effectively with cross-functional team members to support project execution. The role will also collaborate with cross-functional partners, as appropriate, on strategic initiatives. As business needs arise, the role may also provide Medical Affairs support for other investigational programs in collaboration with the TA Lead.

Job Duties and Responsibilities

+ Serves as the medical director for assigned prostate cancer projects, providing medical and scientific leadership in collaboration with the Medical Affairs Director, Solid Tumors TA Lead.

+ Collaborates with the Medical Affairs Director, Solid Tumors TA Lead to develop Medical Affairs strategic plans aligned with brand strategic imperatives and informed by external engagement, MSL and cross-functional input, and actionable insights, supporting data generation, scientific communication, education, and stakeholder awareness.

+ Supports the Medical Affairs Director, Solid Tumors TA Lead in ensuring coordination and alignment of Medical Affairs activities with external alliance partners for assigned projects.

+ Provides medical and scientific input into the development and execution of Medical Affairs plans and scientific platforms.

+ Partners with the U.S. Field Medical team, Medical Communications & Operations, RWE & HEOR, and ex-U.S. colleagues to support cross-functional medical alignment.

+ Supports implementation of plans through multimodal medical education channels, including publications, presentations, congresses, advisory boards, independent medical education, medical symposia, and other channels.

+ Contributes to the development and implementation of detailed scientific publication plans.

+ Engages externally within the medical/scientific community and develops relationships with scientific key opinion leaders, as appropriate to assigned projects.

+ Works with internal cross-functional stakeholders, as appropriate, to bring the medical perspective to internal strategies and tactics.

+ May partner with the Research & Development organization for ongoing and post-development activities and may provide Medical Affairs input to R&D for assigned projects.

+ Attends relevant medical and scientific conferences to support speakers and presenters, publication/communication goals, and the collection and reporting of competitive intelligence within company guidelines.

+ Supports investigator-initiated and collaborative research programs for assigned projects.

+ Contributes to Medical Affairs budget planning and manages assigned project budgets, as appropriate.

+ Ensures that all interactions and activities in the U.S. adhere to corporate and healthcare compliance guidance.

+ As business needs arise, provides Medical Affairs support for other investigational programs in collaboration with the Medical Affairs Director, Solid Tumors TA Lead.

Knowledge, Skills and Abilities (general & technical)

+ Strong understanding of Medical Affairs strategy, scientific communications, publication planning, evidence generation, congress planning, advisory boards, and external expert engagement.

+ Scientific and medical knowledge in oncology.

+ Ability to translate complex scientific and clinical information into clear, actionable medical strategy and communications for internal and external stakeholders.

+ Demonstrated ability to lead cross-functional projects, manage competing priorities, and influence without direct authority in a matrixed environment.

+ Excellent written and verbal communication skills, including the ability to present scientific and strategic information to peers, leadership, and cross-functional partners.

+ Sound judgment, integrity, and strong understanding of healthcare compliance, promotional review, and appropriate scientific exchange.

Education & Experience Requirements

+ Advanced degree in a scientific or healthcare-related field required; PharmD, PhD, MD, DO, or equivalent strongly preferred.

+ Minimum of 8 years of relevant experience in the pharmaceutical, biotechnology, healthcare, or related life sciences industry required.

+ Medical Affairs experience preferred; oncology experience required.

+ Experience supporting medical strategy, scientific communications, publication planning, evidence generation, or field medical collaboration preferred.

+ Experience working with cross-functional teams and external scientific experts in a compliant, highly regulated environment preferred.

Other Requirements (licenses, certifications, specialized training, and physical or mental abilities required)

+ Completion of company-required compliance training is required.

+ The role requires the ability to exercise independent judgment, handle confidential information, communicate scientific information accurately and in compliance with applicable policies, and operate effectively in a fast-paced, matrixed environment.

Travel Requirements

+ Ability to travel domestically and internationally to attend scientific congresses, internal meetings, external stakeholder engagements, and alliance or cross-functional meetings, as business needs require. Travel is expected to be up to 25%.

Mental/Physical Requirements

+ This position is office-based and requires the ability to sit or stand for extended periods, use a computer and standard office equipment, participate in virtual and in-person meetings, read and interpret complex scientific and business documents, and communicate effectively with internal and external stakeholders. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

People Management

+ This role does not have direct people-management responsibilities. The position is expected to provide medic...

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