Posted to MedZilla on 12/5/2019

Takeda Pharmaceuticals

US-MA, Sr Director, Outcomes Research SR0035469-MZ


Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a Sr Director, Outcomes Research in our Lexington, MA 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.


Contribute to the development and execution of U.S. Medical strategies to elucidate unmet clinical, economic, and patient-centered needs and product value.
Create and direct the exploratory data analysis environment that will be utilized to direct product scientific and value strategies and inform outcomes research studies, pipeline products, and business development opportunities
Contribute to the development of value propositions that differentiate assigned products for payers, policymakers, healthcare providers, consumers, and other stakeholders.
Lead multiple work streams relating to OR business areas (e.g., health economic modeling, value communications, observational research, payer partnerships) to a high standard.
Set the strategic direction and guide the evolution of value-based performance metrics leading to value-based contracting options across our portfolio. Responsible for interfacing with customers on the data framework of contracts and for overseeing the analysis output to inform final contractual obligation.
Oversee the strategic and operational statistics activities that support USMO research (MACS, publications, and HEOR)


Work within a multidisciplinary, matrixed organization to support the development and creation of medical and research strategies for assigned therapeutic area(s).
Design and execute approaches to leverage available internal real world data (RWD) to inform the development of value evidence for products.
Develop strategic partnerships across our portfolio on RWD assets, analytics, and technology.
Management, including design, implementation and communication of results of OR research studies that help achieve product-specific objectives.
Represent the OR research function on corporate non-technical, cross-functional teams related to product development and commercialization.
Collaborate and partner with key internal stakeholder colleagues and external key opinion leaders to ensure priorities and strategies are aligned.
Conduct relevant research activities which may include, but not be limited to:

o Longitudinal prospective observational, pragmatic clinical trials, and/or patient registries evaluating clinical, patient-centered, and/or economic endpoints;
o Longitudinal retrospective studies of existing databases to assess patient characteristics, treatment patterns, and associated clinical, economic, and/or patient-reported outcomes;
o Retrospective or prospective evaluations of disease natural history and treatment patterns, including drug utilization and adherence;
o Cross-sectional surveys of patients, caregivers, health care providers/practitioners, and/or payers;
o Assessments exploring burden of illness and/or comparative effectiveness;
o Models of cost-effectiveness and budget impact;
o Evaluation of BTP and adherence programs.

Review outcomes research protocols, statistical analysis plans (SAPs), and reports.
Review, and publish scientific reports reflecting ongoing or completed work.
Communicate with relevant internal and external audiences, which may include regulators, health care providers/practitioners, payers, health systems, patients, and others.
Oversee US strategic and operational statistical support for USMO sponsored Clinical studies, Publications and Outcomes research
Upon request, coordinates and delivers scientific, pharmacoeconomic and disease awareness information as presentations or other forms of scientific exchanges to regionally and nationally based managed care organizations, pharmacy benefits management companies, government payers, health care systems, and other organizations or professionals that are involved with health care policy, disease management/quality improvement, comparative effectiveness, and medication formulary decisions.
Promote effective communication of study findings as appropriate, in conference presentations, publications, dossiers and other means.


Combination of academic training and practical experience in scientific methods is required. This may be consist of:
o Doctoral degree (e.g., Ph.D., Sc.D., or Dr.P.H.) in a relevant discipline such as, but not limited to, health services research, health outcomes research, epidemiology, pharmacy administration, public health, psychology, economics, statistics or decision sciences, plus 8 years practical experience, or
o Clinical degree (e.g., in medicine, pharmacy, nursing) and a masters degree in a related discipline (as noted above), with ten years practical experience, and
o Practical experience (preferred number of years as noted above) in performing applied healthcare research, in any setting, including life sciences company, research organization, academic institution, or governmental agency, is required.
Expert knowledge and experience in management of applied healthcare research in the multi-disciplinary drug development and commercialization environment and process (involving multiple stakeholders) is expected.
Advanced knowledge of analytical approaches and ability to work within structured or unstructured data using statistical and data management software (e.g., SAS, Stata, R, etc.).
Experience analyzing data from traditional healthcare databases (e.g., administrative claims data , electronic medical records, etc.).
Knowledge of clinical research and study design along the continuum of drug development is highly desired.
In-depth knowledge of the U.S. healthcare system is expected.
Demonstrated expertise in applied healthcare research is required.
Demonstrated track record of peer-reviewed scientific publications, dossier development, and strategic, customer-focused OR tool development is expected.
Knowledge of health care reimbursement systems and health economics is highly desired.
Demonstrated experience in conducting or interpreting statistical analysis is highly desired.
Strong leadership capability with proven skills in team building, and motivating and developing people, is expected.
Proven ability to work collaboratively and lead effectively in a matrixed team environment is expected.
Broad experience in collaborating with research partners and in managing multiple tasks and complex projects is expected.
Demonstrated ability to communicate scientific evidence, with strong written and verbal presentation skills, is required.


Takeda is a global company with corporate headquarters in Japan and with Takeda Pharmaceuticals USA headquarters in Deerfield, Illinois, USA.
Travel to meetings (sometimes requiring overnight stays) involving Takeda colleagues, research partners, and/or external stakeholders is a requirement of the position.
This position may be either office or field-based. If field-based, travel to Deerfield will be required approximately twice a month, in addition to a travel commitment of approximately 20 - 25 %.
Some international travel may be required.


  • 401(k) with company match and Annual Retirement Contribution Plan
  • Tuition reimbursement Company match of charitable contributions
  • Health & Wellness programs including onsite flu shots and health screenings
  • Generous time off for vacation and the option to purchase additional vacation days
  • Community Outreach Programs

Empowering Our People to Shine

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Notice to Employment / Recruitment Agents:

Employment / Recruitment agents may only submit candidates for vacancies only if they have written authorization to do so from Shire, a wholly-owned subsidiary of Takeda s Talent Acquisition department. Any agency candidate submission may only be submitted to positions opened to the agency through the specific Agency Portal. Shire, a wholly-owned subsidiary of Takeda will only pay a fee for candidates submitted or presented where there is a fully executed contract in place between the Employment / Recruitment agents and Shire, a wholly-owned subsidiary of Takeda and only if the candidate is submitted via the Agency Portal. Candidates submitted or presented by Employment / Recruitment Agents without a fully executed contract or submitted through this site shall not be deemed to form part of any Engagement for which the Agency may claim remuneration.

Equal Employment Opportunity

Shire, a wholly-owned subsidiary of Takeda, is an Equal Opportunity Employer committed to a diverse workforce. Shire, a wholly-owned subsidiary of Takeda, will not discriminate against any worker or job applicant on the basis of race, color, religion, gender, national origin, ancestry, age, sexual orientation, marital or civil partnership status, pregnancy, gender reassignment, non-job related mental or physical disability, genetic information, veteran status, military service, application for military service, or membership in any other category protected under law.

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Reasonable Accommodations

Shire, a wholly-owned subsidiary of Takeda, is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please call 484-595-8400 and let us know the nature of your request and your contact information.

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