Program Management, Associate Director- Global Oncology
$154.4k - $242.55kTakeda Pharmaceuticals
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 DescriptionJoin Takeda as Program Management, Associate Director- Global Oncology out of Cambridge, MA office. This position provides strategic program management leadership for the operating model supporting global, cross-functional and cross-divisional teams engaged in Oncology Search and Evaluation (S&E) and Business Development (BD) activities. The role is accountable for translating strategic priorities into integrated plans, enabling timely governance and decision-making, and driving execution of critical organizational priorities and deliverables. Responsibilities include integrated BD Core Team planning & process management; collaboration with cross functional business partners to drive effective ways of working; designing and implementing solutions to achieve successful execution; driving the team to identify risks and mitigation strategies, clearly outline issues and establish a path to resolution. This position will need to engage with Leaders as needed to ensure timely decision making and to drive team effectiveness. The Associate Director collaborates with the Oncology Business Unit (OBU) cross functional teams and collaborating functions by providing project management leadership for the planning and execution of cross functional team deliverables. How you will contribute Partners with Business Development (BD) leadership to lead and manage the global, cross-functional OBU BD operating model. They understand the priority focus areas necessary to deliver on the enterprise-wide BD strategy Leads the project planning efforts for BD Search & Evaluation team, BD Core Team, and senior leadership review meetings by defining team priorities in alignment with organizational BD, Commercial & R&D strategies Works closely with BD leadership and is responsible for developing and managing workplans for successful implementation, identification of interdependencies and connections between departments Manage the OBU BD operating model by facilitating meetings based on in depth awareness of program priorities; including agenda planning, material development, action item tracking and follow-up Manage and/or oversee team sites and databases, enabling centralized access to materials, collaboration on shared documents & efficient action item tracking Partners with the cross functional team members to provide financial oversight for OBU BD tactical expenditures, including consolidation, vetting and prioritization of spending risks and opportunities Understands links and dependencies across functions and departments, including planning collaborative initiatives and facilitating smooth coordination and strategic planning among business partners Collaborates with stakeholders to plan, prepare, and follow up on Oncology governance interactions Engages and manages stakeholders across levels and functions, ensuring effective communication. Cross Functional Projects & Program Management Demonstrate strategic thought and resource planning to support multi-geographic projects and engagement of teams working across varying geographies. Drive the rigor with which we manage projects using project management best practices. Ensure that tactical execution and related budget plans—in collaboration with Finance—are developed and maintained and that information is effectively utilized by relevant teams Identify issues and obstacles that could impact the timely completion of priority deliverables and address them with team members and/or escalates to the relevant functional management. Identify and communicate opportunities for change; motivates and enables the team to meet new challenges. As a member of the OBU PMO, provide program management expertise and ad hoc project-based support for enterprise initiatives Minimum Qualifications Bachelor’s Degree science or business-related field requiredExperience 5 to 7 years experience as a project manager leading complex pharmaceutical projects in a multi-disciplinary, global environmentMinimum of 5 years people management experience (direct or indirect) and/or proven leadership experience with a global, matrix team. Demonstrated previous experience as a project manager leading complex pharmaceutical project deliverables and teams in a multi-disciplinary, global environment Experience in intercultural collaboration Proven leadership skills and strategic problem-solving ability Proven ability to communicate clearly and present key information objectively and collaborate effectively with management Demonstrated ability to clearly and concisely communicate/ prepare presentations for audiences at all levels Business Development and/or alliance/external partner management experience highly preferred Knowledge and Skills Project leadership and management skills are required Strong Influencing Skills Ability to foster teamwork by actively participating in and supporting an environment that cultivates professional growth and organizational effectiveness. Ability to independently identify issues and to propose and execute on suitable resolutions Ability to establish impactful improvements to cross-functional processes which impact cross-functional teams Ability to drive decision-making within a cross-functional and cross-cultural, global team structure Flexibility, tolerance and diplomacy to best manage change and differing opinions. Ability to work in a highly complex, multi-cultural, often stressful environment Excellent organizational skills Proven ability to work effectively and diplomatically in conflict situations Smartsheet or similar project management tool, Excel, PowerPoint & Word Ability to develop complex project plans to guide project teams and effectively communicate project timelines and interdependencies Fluent in English Ability to accommodate occasional non-standard work hours due to Global teams working in multiple time zones Travel Requirement- 10% 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.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 SummaryWe 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, MAU.S. Base Salary Range:$154,400.00 - $242,550.00The 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. For information about our benefits, please click here.EEO StatementTakeda 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.LocationsBoston, MAWorker TypeEmployeeWorker Sub-TypeRegularTime TypeFull timeJob ExemptYesIt 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.Reference: R0192989
$139.43k - $232.38k
Associate Director, Global Program Management (Oncology)At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our...SuggestedFull timeLocal area$169.4k - $266.2k
...the role:As a member of Takeda Oncology, your work will contribute to... ...your best. As part of the Global Medical Affairs Oncology team... ...developing and updating training programs, and establishing... ...with cross-function teamsVendor management experienceStrong communication...SuggestedMinimum wageLocal areaRemote work$154.4k - $242.55k
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...knowledge.Job DescriptionAs part of the Global Medical Affairs Oncology team, you will report to the... ...amplification of data. You will also manage agency partners, publication systems,... ...point of accountability for assigned programs.How You Will ContributeDevelop and execute...SuggestedMinimum wageLocal areaRemote work- ...Title: Associate Director, Global Regulatory Affairs Company: Ipsen Biopharmaceuticals... ...three therapeutic areas: Oncology, Rare Disease and... ...regulatory strategies for assigned programs within the portfolio,... ...project team and senior management decision making....SuggestedLocal areaWorldwide
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...you and empower you to shine? Join us as an Associate Director, Global Regulatory Project Management and Strategic Planning - Oncology TAU within our Global Regulatory Affairs... ...ensure global regulatory project plans for programs / products are established and maintained,...Minimum wageFull timeLocal areaRemote workWorldwide$154.4k - $242.55k
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...shine? Join us as an Associate Director, Tumor Genomics and Targeted... ...work. Certified as a Global Top Employer, we offer... ...leader within the Oncology Computational Biology... ...actionable and aligned with program needs.Develop reusable... ...analytical workflows.Manage competing program...Minimum wageWork at officeLocal areaRemote work$182k - $216k
...need, particularly in rare oncology and neurology.Our... ...industry. Role SummaryThe Associate Director, Congress Portfolio Management plays a pivotal role in... ...partners across US and Global Medical Affairs, cross-functional... ..., or strategic program management within the pharmaceutical...Temporary workRemote workFlexible hours$154k - $183k
...are Servier Group, a unique global organization headquartered in... ...multiple medicines approved in oncology, cardiology, and other... ...transformation, and lifecycle management — enabling manufacturing robustness... ...clinical and commercial programs forLinker-Payload chemistry and...Full timeContract workTemporary workRemote workFlexible hours$160k - $250k
...to receive an alert: Create Alert Associate Director, Global Search & Evaluation Facility: Business... ...~ Proven track‑record of project management, search and evaluation, business development... ...in Company employee benefit programs including: ~ Medical ~ Dental and...Local areaFlexible hours- ...Pharma Co., Ltd., is a global pharmaceutical... ...addressing patient needs in oncology, urology, women's... ...Job Overview The Associate Director, Biostatistics reports... ...clinical development programs. This position provides... ...functional decisions, and manage multiple priorities...Full timeWork at officeRemote work
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The Associate Director, Statistical Programming is responsible for statistical programming activities in support... ...access needs.Works closely with Data Management on cross-functional data review... ...lead the creation and validation of global macros or systems that streamline...Full timeTemporary workLocal areaFlexible hours$154.4k - $242.55k
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...experienced programmer to join us as Associate Director, Statistical Programming. This is a critical role... ...results in a timely and accurate manner Manage multiple projects simultaneously, ensuring... ...with ICH/GCP guidelines and global regulatory submission requirements...Full timeContract workLocal areaFlexible hours3 days per week$154.4k - $242.55k
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...seeking a highly motivated Associate Director with strong... ...strategic experience in oncology research to join our... ...record of successful team management skills, preferably... ...industry drug discovery programs, from target... ...site: Our newly opened global research hub in the heart...Hourly payTemporary workWork at officeImmediate startFlexible hours3 days per week$149.33k - $248.88k
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Cookie NoticeAssociate Director, Incentive... ...page is loaded## Associate Director, Incentive... ...Ipsen is a mid-sized global biopharmaceutical... ...therapeutic areas: Oncology, Rare Disease and... ...oversees the incentive programs for the full US... ...Units. This role manages the process for designing...Temporary workFlexible hours$180k - $250k
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Job title: Associate Director, Global Medical Affairs - Dermatology Location: Morristown, NJ About... ...both established and investigational programs. Join the engine of Sanofi’s mission... ...influencing, collaboration, and stakeholder-management skills. Demonstrated ability to...Local area
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