Director, Outcomes Research - Psoriasis
Lexington, MassachusettsAt Takeda, it's our people, our values and our culture that make us special. We share a sense of vocation and a desire to serve others that pulses through our entire organization. We're fortunate to be grounded in a history that gives us a long term perspective, the confidence to stick to what we believe in, and the humility to know we don't have all the answers.
We combine this outlook with an agility and tenacity to deliver for our patients that has fueled the growth of our business. But what really sets our company apart is something we call Patient Trust Reputation Business. It's the framework that enables us to translate our purpose and values into action. It's how we synchronize the diversity of our perspectives, strengths and expertise. And it’s what keeps our decision making tethered to what really matters.
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Job Description
About the role:
Join Takeda as a Director, Outcomes Research (OR) where you will develop and execute health economics and outcomes research for the Gastrointestinal & Inflammation (GI2) Therapeutic Area. As a member of the U.S. OR team, you will identify and implement best practices, design and execute outcomes research to generate real world evidence aligned with strategic objectives and needs to support the GI2 therapeutic area (i.e., psoriasis) and contribute to the development of a best-in-class OR group, focused on U.S., evidence and health economic needs. As part of the US Medical team, you will report to the Sr. Director Outcomes Research and Data Science. This is a hybrid role based in Lexington, MA.
How you will contribute:
Lead and contribute to the U.S. OR strategy work streams for GI2 marketed and pipeline products as it relates to real-world evidence generation, health economic modeling, value communication, observational research, pragmatic real-world evidence trials, and field tool development, etc. to a high standard and business impact.
Work with the GI2 Product Unit teams to understand overall medical strategies and build research/evidence plans that fit within internal cross functional brand and external stakeholder needs (Health Care Providers, Payers, Policy Makers, Patients, etc.)
Lead, conduct and deliver methodologically robust yet feasible studies for priority U.S. HEOR evidence needs.
You will take the HEOR/ real-world research from concept to publication. You will oversee, contribute, and manage study quality, resources, project plan, budgets, vendors and editing scientific content.
Anticipate payer needs, represent the payer perspective/voice, and provide collected payer insights to applicable cross-functional teams thereby optimizing the lifecycle of Inflammation products.
Work closely with our strategic partners within and Outcomes Research:
Value Access Insights and Solutions Team to provide advanced scientific support to medical/OR related field tool and appropriate dissemination of outcomes research studies
Data Science/OR team to conduct exploratory analyses and design potential concepts/tools/initiatives for collaboration with key regionally and nationally based managed care organizations, pharmacy benefit management, government payers and other organized customer groups
Field-based Payer Account Medical Leads (AMLs) team to help drive overall collaborations and effective payer medical interactions.
As possible explore collaborative research or similar partnership projects with national, regional or corporate payer account regarding the demonstration of products overall value, evidence needs or other mutually defined areas of medical/HEOR interest
Work with the Senior Director OR for the Gastrointestinal TA, and cross functionally with US Medical Unit team members, Market Access and Channel function, and franchise marketing/brand teams to facilitate in-depth scientific HEOR knowledge, product value, and strategy development.
Responsible for developing, executing, and publishing outcomes research following Takeda policies and in cooperation with the US Medical Affairs Team.
Manage, lead and conduct relevant research activities which may include, but not be limited to:
Longitudinal retrospective studies of existing databases to assess patient characteristics, treatment patterns, and associated clinical, economic and/or patient-reported outcomes Longitudinal prospective observational, pragmatic clinical trials, and/or patient registries evaluating clinical, patient-centered, and/or economic endpoints;
Retrospective or prospective evaluations of disease natural history and treatment patterns, including drug utilization and adherence;
Cross-sectional surveys of patients, caregivers, health care providers/practitioners, and/or payers;
Assessments exploring the burden of illness, patient preference studies and/or comparative effectiveness;
Models of cost-effectiveness and budget impact; indirect treatment comparison models and methodologies
Maintain a high level of knowledge with regards to the scientific, clinical and commercial developments in the Gastrointestinal therapeutic areas as well as a robust understanding of pharmacy management/medical policy trends/techniques used by payers to make informed decisions about payer strategy and OR plans and tactics
Attend and participate in relevant outcomes-related sessions at scientific and professional meetings. Creates and communicates outcomes-related sessions at scientific and professional meetings that are of strategic interest to Takeda.
Attend and participate in relevant HEOR, outcomes research, pricing, comparative effectiveness, policy and value meetings or symposia that are of strategic interest to Takeda (e.g., ISPOR, ICER, AMCP, etc.) and create reports and communicate reports from these meetings.
Track and report on changes in the healthcare environment that are of relevance to Takeda
Complete all required training, activity documentation, knowledge management systems, expense reporting, and other administrative responsibilities as required by SOPs and guidelines.
Minimum Requirements/Qualifications:
Required:
You will have a doctoral degree in a health sciences related field such as a PharmD, MD or PhD, with a thorough grasp of the pharmaceutical industry, healthcare environment, and outcomes research.
You will be an experienced health economics, health services, and/or outcomes research scientist, with a strong, proven track record of generating evidence to support market access for pharmaceuticals.
Eight years post-doctoral healthcare experience in the pharmaceutical, managed care, or consulting industries with a primary focus on health economics and outcomes research, and an emphasis on Market Access (public or private payers).
Proven track record of teamwork, leadership, project management, timely decision-making and results orientation in meeting business objectives.
Excel at leveraging professional relationships with regionally and nationally based managed care organizations and thought leaders in the areas of pharmacoeconomic and outcomes research and other areas of mutual interest by aligning thought leader expertise with Takeda needs.
Have superior communication skills, both oral and written, and able to engender trust and respect of peers, subordinates and superiors.
Proven business and analytical skills and an in-depth understanding of pharmaceutical business practices that impact commercialized and development of compounds.
Demonstrate expert awareness and the ability to understand, interpret and make recommendations concerning the evolving US health care marketplace.
Desired:
MBA, MPH, MHA or other business training will be considered if degree is specific to health economics or outcomes research, with appropriate clinical background and years of experience.
Health Economic or similar training (e.g., MS, PhD), fellowship, and/or background in outcomes research.
Travel Requirements:
Willingness to travel to various meetings or client sites, including overnight trips and some weekend commitments. Some international travel may be required.
Requires approximately 20% travel, including some overnight and weekend commitments.
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.
Certified as a Global Top Employer, 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 Summary
We 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:
Lexington, MAU.S. Base Salary Range:
169,400.00 - 266,200.00The 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-termincentives. 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 Statement
Takeda 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
Lexington, MAWorker Type
EmployeeWorker Sub-Type
RegularTime Type
Full timeJob Exempt
YesWorking at Takeda
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