Takeda Pharmaceuticals
Senior Director, Clinical Data Management (Oncology & Cell Therapy)
Takeda Pharmaceuticals, Boston, Massachusetts, us, 02298
Are you looking for a patient-focused company to inspire you and support your career? If so, be empowered to take charge of your future at Takeda. Join us as the Senior Director, Clinical Data Management (Oncology & Cell Therapy) reporting to the Head of Clinical Data Management based 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 work towards their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers and work towards 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.GOALS:
Effective leadership, strategic planning, and oversight for one or several Therapeutic Area Units (TAUs) and/or operational units within Clinical Data Management (CDM).Set the vision, direction, and strategy for area(s) of responsibility and actively contribute to and align with the overall CDM, Global Integrated Clinical Trial Data Services, and Global Development Organization (GDO) strategies and operating models. Lead operationalization activities to ensure on time, high quality and within budget delivery that enable successful trial data analyses for Takeda to deliver medicines to patients faster.Champion CDM operational excellence by leading and developing flexible, scalable and innovative methods to internalize key CDM capabilities.An accomplished people and relationship manager, who will establish and maintain productive partnerships within CDM, functional leaders across R&D, and third-party service providers.ACCOUNTABILITIES:
Accountable for the timely and high-quality delivery of clinical databases for assigned TAUs, ensuring fitness of purpose and compliance to applicable regulations and SOPs. Proactively drive quality, efficiency, and innovation to ensure data management deliverables are met within the established timelines, budget, and applicable standards.Lead the development of robust strategies for DM resourcing, outsourcing, technologies and risk management to enable more efficient management, collaboration, and pro-active decision making.Contribute to the overall strategic direction of Takeda R&D and the role of clinical data management in maintaining the company’s competitive advantage and delivering on Takeda’s business objectives.Support the Head of Clinical Data Management in leading cross-functional efforts to build out processes and infrastructure necessary to internalize key CDM capabilities and optimize overall operational delivery. Represent CDM on key cross-functional initiatives.Drive significant levels of business change, within CDM and across the broader organization to ensure the successful execution of the CDM strategy and operating models.Champion harmonization efforts across regions, TAUs and service providers.Recruit, select, develop, manage, motivate, coach and appraise the performance of direct reports. Build team commitment to goals, and create a positive and productive culture within the team. Ensure appropriate training and be a leader and mentor for all DM globally.Lead the development of SOPs, procedural documentation and continuous process improvement activities in collaboration with DM leadership team. Identify areas for simplification and innovation as well as new and emerging enabling technologies.Represent CDM in global regulatory audits and inspections and ensure successful outcomes in line with business expectations.Establish, foster and enhance relationships within and across the global organization as well as with service providers.Be a deputy for the Head, Clinical Data Management as needed.Other responsibilities as assigned.EDUCATION & EXPERIENCE:
Bachelor’s/MS Degree or international equivalent preferred, or equivalent combination of education, training and experience.15+ years of experience with degree, or equivalency of 20+ plus years experience in lieu of degree.7+ years of line management experience with prior second-level management experience required.Successful experience managing operational vendor relationships and alliance partnerships at a program or portfolio level.Proven track record of strong project management skills and experience managing data management activities for large drug development programs.Requires advanced experience working on Phase I-IV studies across multiple therapeutic areas and programs, and be capable of leading DM activities to support regulatory submissions and inspections.Excellent verbal/written communication skills and ability to influence at all levels across functions and build effective relationships.Seasoned leader with a passion for people development and an ability to perform in a highly dynamic environment.Exceptional interpersonal skills, outstanding negotiation and problem-solving skills.Focused and versatile leader who excels under pressure, ambiguity, frequent change, or unpredictability.Entrepreneurial and innovative; takes measured risks; thinks outside the box; challenge the status quo.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:
$205,100.00 - $322,300.00The 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.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 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.Locations
Boston, MAWorker Type
EmployeeWorker Sub-Type
RegularTime Type
Full time
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Better Health and a Brighter Future
to people around the world.Here, you will be a vital contributor to our inspiring, bold mission.GOALS:
Effective leadership, strategic planning, and oversight for one or several Therapeutic Area Units (TAUs) and/or operational units within Clinical Data Management (CDM).Set the vision, direction, and strategy for area(s) of responsibility and actively contribute to and align with the overall CDM, Global Integrated Clinical Trial Data Services, and Global Development Organization (GDO) strategies and operating models. Lead operationalization activities to ensure on time, high quality and within budget delivery that enable successful trial data analyses for Takeda to deliver medicines to patients faster.Champion CDM operational excellence by leading and developing flexible, scalable and innovative methods to internalize key CDM capabilities.An accomplished people and relationship manager, who will establish and maintain productive partnerships within CDM, functional leaders across R&D, and third-party service providers.ACCOUNTABILITIES:
Accountable for the timely and high-quality delivery of clinical databases for assigned TAUs, ensuring fitness of purpose and compliance to applicable regulations and SOPs. Proactively drive quality, efficiency, and innovation to ensure data management deliverables are met within the established timelines, budget, and applicable standards.Lead the development of robust strategies for DM resourcing, outsourcing, technologies and risk management to enable more efficient management, collaboration, and pro-active decision making.Contribute to the overall strategic direction of Takeda R&D and the role of clinical data management in maintaining the company’s competitive advantage and delivering on Takeda’s business objectives.Support the Head of Clinical Data Management in leading cross-functional efforts to build out processes and infrastructure necessary to internalize key CDM capabilities and optimize overall operational delivery. Represent CDM on key cross-functional initiatives.Drive significant levels of business change, within CDM and across the broader organization to ensure the successful execution of the CDM strategy and operating models.Champion harmonization efforts across regions, TAUs and service providers.Recruit, select, develop, manage, motivate, coach and appraise the performance of direct reports. Build team commitment to goals, and create a positive and productive culture within the team. Ensure appropriate training and be a leader and mentor for all DM globally.Lead the development of SOPs, procedural documentation and continuous process improvement activities in collaboration with DM leadership team. Identify areas for simplification and innovation as well as new and emerging enabling technologies.Represent CDM in global regulatory audits and inspections and ensure successful outcomes in line with business expectations.Establish, foster and enhance relationships within and across the global organization as well as with service providers.Be a deputy for the Head, Clinical Data Management as needed.Other responsibilities as assigned.EDUCATION & EXPERIENCE:
Bachelor’s/MS Degree or international equivalent preferred, or equivalent combination of education, training and experience.15+ years of experience with degree, or equivalency of 20+ plus years experience in lieu of degree.7+ years of line management experience with prior second-level management experience required.Successful experience managing operational vendor relationships and alliance partnerships at a program or portfolio level.Proven track record of strong project management skills and experience managing data management activities for large drug development programs.Requires advanced experience working on Phase I-IV studies across multiple therapeutic areas and programs, and be capable of leading DM activities to support regulatory submissions and inspections.Excellent verbal/written communication skills and ability to influence at all levels across functions and build effective relationships.Seasoned leader with a passion for people development and an ability to perform in a highly dynamic environment.Exceptional interpersonal skills, outstanding negotiation and problem-solving skills.Focused and versatile leader who excels under pressure, ambiguity, frequent change, or unpredictability.Entrepreneurial and innovative; takes measured risks; thinks outside the box; challenge the status quo.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:
$205,100.00 - $322,300.00The 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.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 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.Locations
Boston, MAWorker Type
EmployeeWorker Sub-Type
RegularTime Type
Full time
#J-18808-Ljbffr