Senior Clinical Operations Manager - Cell Therapies

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 DescriptionAre you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine?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: The Senior Clinical Operations Manager will lead study operational strategy and planning and oversee execution of clinical studies for Takeda''s cell therapy projects, supporting clinical strategy defined in Clinical Development close collaboration with the Global Project Leader, Clinical Operations Leader, and other key functions, the COM will:Oversee the execution of studies in compliance with quality standards (including ICH GCP, local regulations and Takeda SOPs), on schedule and on budgetOversee Strategic Partners and/or other CROs and other 3rd party vendors (e.g., labs) to meet Takeda''s obligations described in ICH-GCP and Takeda''s business objectivesFurthermore, the role will engage with the broader Development Operations community within Takeda and participate in global initiatives representing Development Operations in support of Takeda R&D objectives.ACCOUNTABILITIES: Accountable for planning and operational strategy and execution for cell therapy stud(ies)Provides subject matter expertise and operational input into protocol synopsis, final protocol and other study related documentsChallenges study team to ensure operational feasibility, inclusive of patient and site burdenValidates budget and ensures impacts are adequately addressedParticipates in country and site feasibility/selection process, with a focus on providing country insights, corporate alignment and therapeutic expertise to ensure alignment between study execution plan and program strategyChallenges study team to ensure timelines meet the needs of the clinical development plan Ensure new team members and vendors are appropriately onboardedDuring Early Engagement with Strategic Partner(s) and/or other CROs, lead the development of the Operational Strategy in preparation for Operational Strategy Review; focus on ensuring accurate assumptions are applied and robust risk management plans are in placeProvide oversight/support/guidance to Strategic partners/CRO to ensure study issues are addressed and resolved rapidlyResponsible for study budget planning and management and accountable for external spend related to study execution. Works closely with the Clinical Operations Leader, Global Program Management, and Finance to ensure on a regular basis that budgets, enrollment, and gating are accurate; Communicates study status, cost and issues to Clinical Operations Program Leader; serve as escalation point for third party vendors managed by Strategic Partner and/or other CROsOversee Strategic Partners/CRO/vendor selection, budget and contract negotiation, and proper supervision of performance for all activities assigned to a Strategic Partner/CRO/vendor, including escalation of issues to governance committees when warranted;Specific areas of responsibilities include, but are not limited to:Review and approval of key monitoring documents/plans, periodic review of outputs, decisions and actions related to monitoringReview and endorsement of relevant study plans, as applicableStudy team meeting management and attendance when necessary; regular review of meeting agendas and minutesReview of outcomes/actions related to protocol deviations review; primary purpose of review is to support the identification of trends across sites and/or the studyDocumented review and monitoring of issues, risks and decisions at the study level and implementation of appropriate mitigation strategiesIn partnership with data management, review and pressure test all database timelines and plans; review and clean data; ensure strong linkage between the strategy (i.e., filing/registration, data generation, etc.) with the tactical plan for database lock and CSREnsure studies are "inspection ready" at all times; may be involved in regulatory inspections by preparing for and/or attending the inspectionsRepresent the Clinical Operations Manager role in functional initiatives or working groups Help onboard / mentor more junior COMsMay assist the program Clinical Program Leader in his/her role, as requiredEDUCATION, EXPERIENCE, KNOWLEDGE AND SKILLS: Education: Bachelor''s Degree or international equivalent required, Life Sciences preferredRequired: 6+ years'' experience in pharmaceutical industry and/or clinical research organization, including 4+ years clinical study managementExperience must include either early phase clinical studies or Phase 2 and 3 studies and global/international studies or programs. Oncology experience required, cell therapy experience preferredStrong knowledge of clinical study reporting requirementsSolid understanding of clinical trial documents (protocols, statistical analysis plans, CRFs, study reports) and processesAdvanced knowledge of medical terminology, medical coding, laboratory reference ranges, clinical diagnostic procedures, anatomy/physiology and nature of disease processesKnowledge in global regulatory and compliance requirements for clinical research, including but not limited to US CFR, EU CTD, and ICH GCP. Awareness of local country requirements is also requiredDemonstrated excellence in project/program management and matrix leadershipKnowledge and Skills:Experience with project leadership and management systems and methodologyMulti-faceted background with direct involvement or experience working with functions from multiple divisionsExpert knowledge in the overall pharmaceutical drug development processDemonstrated ability to build consensus and drive resolution of issues while maintaining positive working relationships across functions; negotiation and strong persuasive abilitiesStrong written and verbal Communication Skills: ability to express oneself clearly and concisely to external partners, vendors or with others within the team; ability to message key issues appropriately and document issues and/or concerns concisely and comprehensively; ability to adjust language and/or terminology appropriate for the audience; demonstrated ability to clearly and concisely communicate / present key information to senior managementAnalytical and Problem Solving Skills: ability to identify the critical issues of problems or opportunities using appropriate information; determines the causes and possible solutions to the problemStrategic Implementation: ability to develop, implement and monitor the overall clinical operations strategyLeadership Skills: develops and uses knowledge and interpersonal skills to influence and guide others towards the accomplishment of Takeda''s goals and objectives; requires the flexibility and tolerance to best manage change and differing opinions with diplomacy and competenceAbility to drive decision-making within a cross-functional, cross-divisional and cross-cultural, global team structure and requires global mindset and cultural awareness in working with senior leadership in other regions and in managing cross-regional projectsAbility to adapt to other personalities in a respectful manner that is conducive to goal achievementAbility to capture knowledge within the cross-functional, cross-divisional global organization; improve solutions, processes, and deliverables through use of information; improve information capital by contributing experience, theories, deliverables, and models for others to useManagement of multiple tasks of varied complexity simultaneouslyAbility to work in a demanding environment with aggressive project timelinesTRAVEL REQUIREMENTS:Willingness to travel to various meetings or client sites, including overnight trips. Some international travel may be requiredRequires approximately 10-15% travelWHAT TAKEDA CAN OFFER YOU: 401(k) with company match and Annual Retirement Contribution PlanTuition reimbursement Company match of charitable contributionsHealth & Wellness programs including onsite flu shots and health screeningsGenerous time off for vacation and the option to purchase additional vacation daysCommunity Outreach ProgramsTakeda 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 accordance with the CO Equal Pay Act, Colorado Applicants Are Not Permitted to Apply.LI-JT1EEO 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.LocationsMassachusetts - VirtualWorker TypeEmployeeWorker Sub-TypeRegularTime TypeFull time LI-Remote

Created: 2025-11-15