Associate Director, Global Program Management

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Job DescriptionAre you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a (Title) in our Cambridge office.
At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to realize their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation, and strive for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.
Here, you will be a vital contributor to our inspiring, bold mission.
OBJECTIVES: Demonstrates excellence in project management in support of one or more drug development programs across all phases of development. Serves as a partner for the Global Project Leader in developing the asset strategy and ensuring efficient execution of tactical plans by the Global Product Team (GPT).
Core responsibilities include:Providing strategic direction and translating the integrated GPT asset strategy into an efficiently executable plan; predicting and planning solutions to achieve program goals and objectives; driving clarity and removing barriers to ensure team success;Interfacing with management and influencing asset-level decision-making;Proactive management and mitigation of development risks, and supporting appropriate communication and interface with enterprise-level governance;Maintaining up-to-date and accurate key program information in PM business systems and ensuring quality program timelines, team data, and required tools are updated as appropriate;Play a key role in ensuring team effectiveness, partnering with GPL and CoOP to administer team health checks to generate insights, plan & execute appropriate follow-up actions;Accountable for asset-level financial management, budget, forecasting, and monitoring of variance.Considered a department wide PM SME, driving cross-divisional alignment and continuous improvement activities.Participates in innovative departmental process improvement initiatives with significant organizational impact and manages, as needed, non-project responsibilities, which can include process and system optimizations.Partners with GPL to lead GPT or Joint Development Team (for partnered Alliance programs) to develop and maintain the asset strategy and corresponding operational development plans in alignment with the ONEOncology strategy, lifecycle management requirements, and evidence generation/publication needs.
Drives delivery of critical path activities to progress asset development. Identifies ways to optimize program execution without compromise to patients or compliance.
Ensures asset strategy and integrated development plan have a patient-centric focus, incorporates innovative approaches that are meaningful to patients, HCPs, regulators & payers, and adhere to the highest standards of operational excellence in drug development and life cycle management. Serves as facilitator and driver of GPT to ensure progress of asset development. This includes establishing meeting agendas in partnership with GPL and GPT members, facilitating effective team discussions, driving to clear and timely team actions and decisions, holding team members accountable for action follow-through. Ensures team effectiveness through team health checks with development and appropriate follow-through on action plans to boost team productivity. Partners with the GPL and program finance lead to provide financial oversight of the program including global, cross-divisional budgets. Includes consolidation, vetting and prioritization of GPT spending to deliver critical path activities.
Leverages team members to proactively identify potential issues or obstacles and achieves resolution or plans contingencies. Follow issues through to resolution ensuring that all key stakeholders are informed of outcomes and program implications. Proactively addresses and removes barriers to program progress, keeping leadership informed of critical considerations (e.g., resources, performance). Provides clarity and direction in urgent or unexpected situations. Independently resolves complex issues and competing priorities that may impact achievement of goals, creates mitigation plans and drives to resolution.
Manages scheduled and ad-hoc program status reporting, citing progress against program goals/KPIs, proactively identifying risk with planned mitigation(s), and providing rationale for timeline and budget variances. Participate in portfolio analyses to communicate program development progress, opportunities, and risks to Senior & Executive Management. Responsible for leading preparation efforts for governance engagement to support and drive asset objectives and deliverables. Facilitates relevant communications to appropriate stakeholders and in conjunction with Alliance Managers, with Alliance partners.
Considered a department–wide PM SME, driving cross-divisional alignment and continuous improvement activities. May participate in initiatives that have cross-functional or cross-divisional impact that are critical to the objectives of the Therapeutic Area Unit (TAU), Center of Operational Performance (CoOP), and/or global business objectives.
EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS: Bachelor's Degree in science or business-related fieldAdvanced degree in science or business is preferredPreferred: 5-7 years of in-depth pharmaceutical industry experience and drug development in all phases of development with significant experience within related functions (e.g. Clinical Science, Clinical Operations, Research, Regulatory, CMC, Marketing)3-5 years program management experience leading complex pharmaceutical projects in a multi-disciplinary, global environmentDemonstrated ability to positively influence outcomes, key project decisions, and strategic problem-solvingProven ability to communicate clearly and present key information objectively to all levels of the organization including executive managementMatrix program leadership and management skills are requiredThorough knowledge of Therapeutic Area preferable but not requiredAbility to influence and negotiate in a matrix environment to optimize development and address barriersProactive risk management with ability to propose solutions and deliver appropriate mitigation planAbility to communicate (written and verbal) with impact to provide appropriate context, articulate views, drive clarity, and address barriers to progress program developmentAbility to drive decision-making within a cross-functional and cross-cultural, global team structureFlexibility, tolerance and diplomacy to best manage change and differing opinionsAbility to work in a virtual setting/across time-zones, i.e., making effective use of communication tools (WebEx, TelePresence, telephone and video conferencing, etc.)Ability to inspire and motivate in a matrix and global, cross-geographical teamAbility to work in a highly complex, multi-cultural, environmentExcellent organizational skillsA solid business background as well as excellent commercial understandingHighly effective presentation skillsExperience with Microsoft Project Professional, SharePoint, Excel, PowerPoint & WordTakeda 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.
This position is currently classified as "hybrid" in accordance with Takeda's Hybrid and Remote Work policy.
LocationsBoston, MA
Worker TypeEmployee
Worker Sub-TypeRegular
Time TypeFull time

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