Director, US Medical – HAE, Rare Disease

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Job Description

About the role:

Join Takeda as a Director, US Medical – HAE, Rare Disease where you will have product level strategic responsibility for one or more products and may have broader responsibility for later in lifecycle TA. You will also be accountable for medical strategy, ensuring that TA and product-specific strategies are developed and executed in collaboration with the Medical Unit. You will be a Subject Matter Expert (SME), representing the USMA at the Global level for a product on relevant internal committees. You will be accountable for the relevant budget, and coaches/mentors team managers, as appropriate. Further, the Director drives overall medical unit insights, including ad boards, and communication with cross-functional partners. This is a critical role within the US Medical Affairs (USMA) organization that reports to the Senior Director – US Medical Head, Rare Immunology. This is a hybrid role based in Lexington, MA.

How you will contribute:

Overarching Responsibilities:

• Product Level strategic responsibility for one or more products, may have broader responsibility for later in lifecycle TAs.

• TA and/or product focus may evolve to support priorities of the organization (e.g. additional TA or product-specific responsibilities may change based upon the strategic direction of the organization).

• Oversee and/or delegate the execution of medical strategies by the medical unit partner with the PM to track progress against strategic plans, including development + communication of periodic reports.

Develop US Product Medical Strategy:

• Lead/co-develop/coordinate with the medical unit and provide medical input into the near-term and long-term strategic direction for assigned product.

• Accountable for the development and ongoing updates to relevant product specific medical strategies, in partnership with medical unit, and in alignment with the commercial brand strategy and global product teams.

• Collaborate with Value and Evidence Generation team to develop evidence generation strategy.

• Develop long-term lifecycle management strategy + tactics (HEOR etc.) 

• Collaborate with PM (as applicable) to develop and maintain the medical landscape and insights to inform strategy.

Team Management:

• Manage Associate Directors (aligned with Sr. Director), to effectively develop and execute medical strategy, including delegation of responsibilities, providing ongoing oversight and coaching to ensure the team is achieving the objectives of the medical strategy (as applicable).

Medical Expert:

• Serve as the in-house medical and scientific expert for therapies within the assigned TA and represent medical affairs at the Global level for a product.

• Generate Insights – Develop and execute ad board strategy, which may be done in partnership with the PM (as applicable), and insights from field medical/additional sources.

• Understand and Communicate Insights: Synthesize summarized insights + implications from relevant sources (e.g., ad boards, field medical) to the medical unit and cross-functional stakeholders and update medical landscape + medical strategy (as appropriate).

External Engagement:  

• Develop external KOL relationships and insights through Advisory Boards, professional associations/meetings and conferences etc.; manage global interactions with US KOLs and vice-versa.

• Partner with US Strategic Medical Alliances group on external partnership, as appropriate (e.g., external affairs/government affairs).

Budget Management:

• Accountable/Responsible for budget at the Product level, and ongoing budget management in partnership with the PM or delegated to Associate Director, and in concert with Sr. Dir. + TA Head.

• Coordinates with the medical unit and functional leads.

Execution / Content Creation:

• Partner with the medical unit functional leads to ensure strategic alignment related to the execution of the relevant product medical strategy and how it is pulled through into tactics (e.g. Grants, Medical Communications (e.g. SCP, ICP, Slide Decks), Publications, Research, Field Medical, Etc.).

• Support medical review of appropriate materials as part of medical and commercial review processes. 

Internal Engagement:

• Lead/coordinate with the medical unit, including attending regular meetings, and representing on the SLT (assuming most medical units are product-level, but may be broader).

• Represent medical affairs (i.e., be the point of contact) on cross-functional / cross-division meetings (representation on global medical forums, commercial / product forums, NPP, etc.).

• Primary point of contact: Ensure appropriate delegation for TA/product-specific single point of contact for Medical Affairs; [e.g., ensure representation on GPT – R&D, GMA, Commercial Teams (e.g., IBD insights team)].

• Provide input into confidential new business development. 

Leadership Behaviors:

• Demonstrates strategic enterprise thinking finding innovative ways to serve patients, and building trust, reputation, and business.

• Creates an environment that inspires and enables people to move the organization forward.

• Focuses on a few priorities and delivers superior results.

• Elevates the capabilities of the organization for now and the future.

• Demonstrated ability to communicate and influence up, down, and cross-functionally with the ability to influence internally, and externally.

• Executive Presence & strategic storytelling. 

• Ability to oversee and delegate and manage stakeholders.

Minimum Requirements/Qualifications:

Required:

• Advanced Doctoral Degree (e.g., MD, DO, PhD, PharmD). 

• Other advanced degreed professionals considered depending on past relevant pharmaceutical industry experience, and/or clinical work, research, or academic endeavors. 

• Experience with clinical research, publication activities, congress presentations, and public speaking.

Preferred:

• Advanced Doctoral Degree (e.g., MD, DO, PhD, PharmD) preferred with at least 5 years of relevant clinical practice, research, academic and/or pharmaceutical industry experience.

LICENSES/CERTIFICATIONS: Maintain minimum standards of education/certification in individual professional discipline

TRAVEL REQUIREMENTS: Periodic travel required (up to 20%) 

More about us:

At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.

Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.

This position is currently classified as "hybrid" in accordance with Takeda's Hybrid and Remote Work policy.

Takeda Compensation and Benefits Summary

We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices.

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U.S. Base Salary Range:

EEO Statement

Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.

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Job Exempt