Director, Companion Diagnostics Medical Lead, Global Medical Affairs Oncology

Company: Takeda
Location: Boston
Posted on: January 15, 2026

Job Description:

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description About the role: As a member of the Global Medical Affairs Oncology (GMAO) Leadership Team within Takeda’s Oncology Business Unit (OBU), this role is accountable for shaping the global Companion Diagnostics (CDx) and biomarker medical vision, strategy, and execution in support of Takeda’s oncology portfolio. The role leads the development and implementation of holistic, end?to?end CDx Medical Affairs strategies across prioritized molecules and tumor types, ensuring strong alignment with pipeline priorities, precision medicine ambitions, and Takeda’s commitment to bringing transformative medicines to people living with cancer. This leader will partner closely with Global and Regional Oncology Medical Affairs, Precision & Translational Medicine, Global Clinical Development, GEO, Discovery, Business Development, Commercial and Market Access, as well as the Oncology Business Unit Leadership Team and key external partners to accelerate appropriate biomarker testing and CDx adoption worldwide. How you will contribute: Provide strategic leadership for global medical strategy on Companion Diagnostics (CDx) and biomarkers across the Oncology portfolio, driving precision medicine and patient impact. Define enterprise?level CDx and biomarker priorities in collaboration with Medical Affairs, Precision Medicine, Clinical Development, Commercial, Market Access, and other cross?functional partners, ensuring alignment with portfolio and business objectives. Serve as a key advisor to Franchise Heads, Global Medical Affairs Teams (GMATs), Global Medical Affairs Strategy Team (GMST) leads, and regional leaders to enable cohesive, forward?looking decision?making. Influence cross?functional strategies (evidence generation, label expansion, lifecycle management, access/testing pathways) to ensure integrated, patient?centric approaches to biomarker testing and CDx implementation. Leverage AI, digital health, and emerging technologies to inform CDx strategy, identify opportunities, and optimize scenario planning and execution. Lead development and execution of global Medical Affairs strategies for CDx and biomarkers, ensuring readiness, evidence?based decision making, and strong stakeholder alignment. Drive global medical readiness for CDx launches and lifecycle management through early, integrated planning with regions, affiliates, and alliance partners. Identify evidence and educational gaps (e.g., testing rates, assay performance, patient journey barriers) and design targeted strategies such as scientific education, data generation, and collaborative studies. Build and maintain trusted partnerships with external experts, diagnostic companies, laboratories, professional societies, and patient organizations to shape adoption of CDx and biomarker?driven care. Collaborate with global and regional Patient Advocacy Group (PAG) leads to integrate patient/caregiver insights and co?create educational initiatives supporting timely, appropriate testing and treatment decisions. Minimum Requirements/Qualifications: Demonstrated focus on patients’ interest MD, PharmD or PhD 7 years post-doctorate healthcare or related experience 5 years’ experience in pharmaceutical industry with at minimum 3 years of direct companion diagnostics work required. Previous experience with CDx product launch required Willingness and ability to meet and engage HCPs, labs and other direct customers Multiple functions experience is preferred as well as experience in global, region and affiliate level Experience in oncology and/or hematology-oncology preferred. Demonstrated track record of success leading multidisciplinary CDx development teams within a pharmaceutical company Excellent oral, written, and presentation skills, including proven success in communicating ideas to build collaborative work relationships Ability to work effectively in a fast paced, rapidly changing technology environment Strong interpersonal skills particularly motivational, negotiation, listening, judgment, analytic, and conflict management skills, demonstrated by ability to lead teams. Proven skills in negotiation, influencing without authority and working diplomatically through conflict Ability to proactively predict issues and solve problems Proven experience in and understanding of multiple regional/country markets Deep understanding of the brand(s)/therapeutic area and the stakeholders’ needs Experience overseeing and managing budgets to ensure performance versus targets Advanced PC skills, including MS Word, Excel, Power Point, and SharePoint 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. For Location: Boston, MA U.S. Base Salary Range: $191,800.00 - $301,400.00 The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location. U.S. based employees may be eligible for short-term and/ or long-term incentives. U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short-term and long-term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation. 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. Locations Boston, MA Worker Type Employee Worker Sub-Type Regular Time Type Full time Job Exempt Yes It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Keywords: Takeda, Boston , Director, Companion Diagnostics Medical Lead, Global Medical Affairs Oncology, Science, Research & Development , Boston, Massachusetts