Director/Associate Director, Global Medical Evidence Lead

Company: Takeda Pharmaceutical
Location: Cherry Hill
Posted on: January 15, 2023

Job Description:

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Job Description

About the role:
At Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on four therapeutic areas and other targeted investments, we push the boundaries of what is possible in order to bring life-changing therapies to patients worldwide.

Join Takeda as a Director/Associate Director, Global Medical Evidence Lead where you will be responsible for post-approval within the CoE of Global Medical. Leads the development of a strategic integrated evidence generation plan. You will partner with GPT Evidence Generation sub team (a multidisciplinary team), to develop/optimize the integrated strategic evidence generation initiatives across therapeutic areas, proactively anticipating any potential gaps and adjusting tactical plans to address these.

You will also support the development of a strategy for all study types within the CMO, i.e. sponsored studies (MACs), Collaborative research and IIRs. Provide innovative thinking and scientific expertise into post-approval research programs and real-world evidence strategies. As part of the Global Medical Evidence team, you will report to the Head, Global Medical Evidence.

How you will contribute:

• Support strategic discussions for each assigned therapeutic area to identify research gaps and develop aligned strategic and tactical plans to address these gaps. And works closely with GMA GPT representatives and partners responsible for executing evidence generation plan;
• Drive, build and maintain the strategic evidence generation plans, closely partnering with the GML, PVPA and GORE with input from multiple stakeholders (regions, SQS, etc);
• Establish GMA framework (i.e. subteam to asset strategy team) to support evidence generation needs;
• Collaborate with cross-functional team members to define global evidentiary needs of key stakeholders (Regulatory bodies, HCPs, Patients/caregivers, Payers, and HTA bodies) to serve the evolving healthcare environment;
• Support collaborative strategic planning and mapping of evidence generation activities with key internal stakeholders to develop aligned and integrated generation strategies and plans;
• Enhance collaboration between various groups within Takeda through sharing of data and best practices;
• Provide strategic leadership and scientific direction on medical evidence activities in order to set standards for utilization of medical data and maximize patients' access to our innovative medicines;
• Participate as a functional expert on other cross-functional leadership teams. Minimum Requirements/Qualifications:
  • Minimum MS degree required (preferably PhD), preferably in a health sciences related field with 8 years of research related experience and/or pharmaceutical industry experience.
  • Experience with late stage clinical studies, research collaborations and RWE
  • Proven track record of strong leadership, project management and demonstrated ability to coach and mentor individuals.
  • Ability to communicate and interact thoughtfully, transparently, and appropriately with a variety of stakeholders both internal and external to Takeda.
  • Experience overseeing work of and mentoring other individuals with a variety of scientific and non-scientific backgrounds and training
  • Experience working in a global organization and within matrix structure highly desirable What Takeda can offer you:
    • Comprehensive Healthcare: Medical, Dental, and Vision
    • Financial Planning & Stability: 401(k) with company match and Annual Retirement Contribution Plan
    • 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 and company match of charitable contributions
    • Family Planning Support
    • Flexible Work Paths
    • Tuition reimbursement 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.
      
      Base Salary Range: $143,500 - 205,000, based on candidate professional experience level. Employees may also be eligible for Short-term and Long-Term Incentive benefits as well. Employees are eligible to participate in Medical, Dental, Vision, Life Insurance, 401(k), Charitable Contribution Match, Holidays, Personal Days & Vacation, Tuition Reimbursement Program and Paid Volunteer Time Off.
      
      The final salary offered for this position may take into account a number of factors including, but not limited to, location, skills, education, and experience.
      
      In accordance with the CO Equal Pay Act, Colorado Applicants Are Not Permitted to Apply.
      
      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
      
      Boston, MA
      
      Worker Type
      
      Employee
      Worker Sub-Type
      
      Regular
      Time Type
      
      Full time

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