Global Medical Evidence - Integrated Evidence Generation Plan Lead

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Objectives/Purpose

Job Description

• Leads the development of a strategic integrated evidence generation plan for rare diseases, growth and launch brands. Partners with the Global Program Team (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.
• Contributes to the asset strategy through membership on matrix teams and through interactions with cross-functional partners
• Leads the development of peri -and post-approval interventional and RWE prospective study design within the CoE of Global Medical.
• Provides innovative thinking and scientific expertise into peri- and post-approval research programs and real-world evidence strategies.
• Lead and drive discussions at the Evidence Generation Sub-team to relevant internal and external audiences as effectively as possible
• Supports the development of a strategy for all study types within Global Medical, i.e. Medical Affairs Sponsored Studies (MACs). Also, develops Areas of Interest (AOI) for Collaborative research and IIRs.
  
  

SCOPE

• Leads 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;
• Drives, builds and maintains the strategic evidence generation plans, closely partnering with the Global Medical Lead (GML), Global Patient Access (GPA) and Global Evidence and Outcomes (GEO) with input from multiple stakeholders (regions, Statistical and Quantitative Sciences (SQS), etc);
• Establishes GMA framework (i.e. subteam to asset strategy team) to support evidence generation needs;
• Collaborates 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;
• Supports collaborative strategic planning and mapping of evidence generation activities with key internal stakeholders to develop aligned and integrated generation strategies and plans;
• Enhances collaboration between various groups within Takeda through sharing of data and best practices;
• Prepare and review research protocols from regions and LOCs, statistical analysis plans (SAPs), and reports reflecting ongoing or completed work.
• Provides strategic leadership and scientific direction on medical evidence activities in order to:
• Set standards for utilization of medical data.
• Maximize patients’ access to our innovative medicines;
• Participates as a strategic and functional expert on other cross-functional leadership teams.
• Compliance with all policies and SOPs.
• Accountable for product annual plan budget and contract/budget management.
  
  

DIMENSIONS AND ASPECTS

Technical/Functional (Line) Expertise

• Advanced level understanding of research and the pharmaceutical industry
• Advanced knowledge of systems
  
  

Required

EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS:

• Master’s degree required (preferably PhD), preferably in a health sciences related field with 10 years of research related experience and/or pharmaceutical industry experience.
• Strong and effective communication skills absolutely essential
• Experience with late stage clinical studies, research collaborations and RWE. Knowledge of HTA/payor needs
• Proven track record of strong leadership and excellent project management skills including the ability to manage multiple complex research studies
• Ability to collaborate, communicate and interact thoughtfully, transparently, appropriately and effectively with a variety of multicultural stakeholders both internal and external to Takeda.
• Broad experience in collaborating with research partners and in managing multiple tasks and complex projects is very required
• Ability to communicate scientific evidence, with strong written and verbal presentation skills, is required.
• Networking, communication and influencing skills. Ability to lead cross-functional teams.
• Ability to influence without authority, particularly individuals at senior levels
  
  

Desired

• Experience overseeing work of and mentoring other individuals with a variety of scientific and non-scientific backgrounds and training
• Experience working in a large global organization and within matrix structure highly desirable.
  
  

Location:

• Cambridge, MA - Hybrid
  
  

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:

Boston, MA

U.S. Base Salary Range

$174,500.00 - $274,230.00

The 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 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

Job Exempt

Yes

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

If you have questions about this posting, please contact [email protected]