Takeda · 5 hours ago
Director, Global Program Management - Companion Diagnostic-
Boston, MA
Full-time
Hybrid
Lead/Staff, Director/Executive
$174K/yr - $274K/yr
5+ years expTakeda is a patient-focused, innovation-driven company that is transforming the pharmaceutical industry. The Director, Global Program Management will drive efficient and effective companion diagnostic strategy execution for oncology programs, ensuring collaboration with internal stakeholders and external partners to support regulatory submissions and health authority meetings.
BiotechnologyHealth CareManufacturingMedicalPharmaceutical
Responsibilities
Provide operational excellence to the Companion Diagnostic Working Group and Translational Subteam of the Global Program Team
Provide operational support in the development and execution of companion diagnostic strategy including program level deliverables (clinical biomarker and diagnostic plans, data interpretation, collaborations), diagnostic elements of governance presentations; and developing resource recommendations as needed
Collaborate with cross-functional team members to develop and deliver companion diagnostics in alignment with therapeutic programs
Coordinate companion diagnostic program team meetings with internal team members to implement the program CDx strategies. Schedule team meetings, develop agendas, as well as capture minutes and track action items
Support Joint Project Team meetings with external diagnostic partners
Build companion diagnostic project plans, timelines, and risk mitigation strategies for CDx development activities (with both internal team and external diagnostic partner) and work with GPM to implement into broader program plan. Interact with potential diagnostic vendors and clinical sites to support the plan
Contribute to the planning and tracking of program budgets and resource allocations,
Develop project planning documents and archive project materials to ensure visibility of both project history, current status, and future directions
Drive execution of companion diagnostic project plan, including assignment of responsibilities and tracking of internal and external deliverables. Maintain a risk register for companion diagnostic deliverables
Support timely delivery of biomarker data and analyses to drive decision making, project advancement/milestone transitions and resource allocation across functions
Ensure coordination of key decisions and milestones by close collaboration across Translational Scientific Leaders, Companion Diagnostic Leads and key cross-functional stakeholders such as Clinical Operations, Clinical Biomarkers, Clinical Sciences, Oncology Drug Discovery and Regulatory Sciences to successfully deliver, communicate and execute companion diagnostic strategy for projects and platforms
Drive timely decisions and accountability within the team and facilitate active communication and information flow between translational team members, stakeholder functions, and governance bodies
Leverage program management best practices to facilitate cross-functional translational and companion diagnostic team meetings fostering a team culture of transparency, accountability, high cross-functional communication and accountability, and timely execution
Contribute to broader translational matrix by sharing ideas, tools, best practices and lessons learned
Qualification
Required
Master Degree or Ph.D
5-8 years of experience in pharmaceutical drug development with a focus on companion diagnostic development
Strong companion diagnostic development experience required
Broad knowledge of key companion diagnostic deliverables including clinical assay and IUO device development, sample tracking and management, experience working with external partners and contract laboratories, data delivery, project management best practices and proficiency with supporting project management tools
Experience with delivering and overseeing CDx contracts with external partners and vendors
Proven experience managing companion diagnostics or IVD programs
Have background in understanding of drug-diagnostic co-development and regulatory pathways
Experience with biomarker-driven clinical trials and clinical data integration
Understanding of key considerations relevant to global regulatory requirements
Experience developing team culture, resolving conflicts, and driving decision-making in a matrix environment
Teamwork – Ability to work well in a highly cross-functional team environment
Communication - Able to express oneself clearly and concisely within team; documents issues and/or concerns concisely; timely and effectively communicates issues to supervisor and team members
Analytical and problem-solving skills. Able to troubleshoot critical issues or problems, determine causes and determine and implement solutions
Organization – Strong project management skills, exercises good time management/prioritization skills and can successfully manage multiple tasks simultaneously
Motivated – Self-motivated and willing to accept temporary responsibilities outside of initial job description
Benefits
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.
Company
Takeda
Takeda is a biopharmaceutical company that researches and develops pharmaceutical drugs.
10001+ employees
H1B Sponsorship
Takeda has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (34)
2024 (40)
2023 (39)
2022 (34)
2021 (44)
2020 (18)
Funding
Current Stage
Public CompanyTotal Funding
$2.46B2025-06-27Post Ipo Debt· $2.4B
2016-09-01Grant· $19.8M
2016-05-08Grant· $38M
Leadership Team
Christophe Weber
President and CEO
Schuyler Fairfield
Senior Vice President, Global Head of Supply Chain
Recent News
BioWorld Financial Watch
2025-12-21
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