By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.
Job Description
Global Medical Lead, Evidence Generation Rare Hematology
Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a Global Medical Lead, Evidence Generation Rare Hematology in our Cambridge, 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.
As a Global Medical Lead, Evidence Generation Rare Hematology working on the Global Medical Affairs team, you will be empowered to develop and implement Hematology data-generation strategies, and directly implement and execute real world evidence and data-generation plans and collaborate across medical Hematology team. A typical day will include:
POSITION OBJECTIVES:
Work with GMTL, GML and Head GM Hematology to develop and implement Hematology data-generation strategies
Support close alignment with overall strategy and incorporating R&D functional strategies (clinical regulatory, PV, Compliance)
Work across franchise with GMTL and GML and clinical operations, the CMO strategy group, Evidence generations operations group to ensure execution of data-generation projects according to company standards
Support execution of specific medical projects related to RWE per global medical strategy
Serve as Hematology medical representative on standing and project-based cross functional teams
Act as company representative interacting with external scientific leaders, study centers, patient advocacy groups and authorities as needed
Establish appropriate strategic partnerships with centers of excellence and scientific/clinical experts in areas of scientific interest
POSITION ACCOUNTABILITIES:
Managing design, develop protocols and execution of clinical studies (phase IIIb/IV, disease registries, HEOR studies, outcome surveys, etc. in close collaboration with Global Franchise related functions
Work within Global Medical across franchise with global medical team to develop multi-year global medical strategy for data-generation studies and seek alignment for the specified Product/Disease Area appropriately aligned with overall strategy and incorporating R&D functional strategies (clinical , regulatory, HEOR PV, compliance)
Support development of the in-year global medical plan for these projects and budget for respective initiatives
As delegated by the Head GM Hematology, participate in product development strategy and provide medical affairs and R&D inputs
Publication planning in alignment with GML and Publications team
Execution, planning, designing, and managing scientific meetings like advisory boards or Investigator meetings including vendor management and approval processes
Providing medical review of investigator Initiated Research (IIR) proposals and other grants through the applicable process
Managing completion of regulatory obligations (i.e. medical input in safety review teams sd needed)
Monitoring and communication progress against study plan, propose and initiate initiatives as need to adjust timelines ad budget
Represent global medical Hematology in relevant medical, R&D or cross functional teams as needed
Effective, compliant collaborations with internal stakeholders and scientific exchange with external stakeholders in alignment with needs of external stakeholders and medical strategy
EDUCATION, BEHAVIORAL COMPETENCIES AND SKILLS:
A medical degree or PhD with experience in related indications is required
>5 years’ experience in the pharmaceutical industry,
Medical Affairs, clinical development and real world evidence generation experience.
Data-generation related regulatory experience and experience in leading studies, registries, IIR or scientific projects
Ability to work in the global environment
Ability to represent the company’s interest in scientific forums as needed
This job posting exclude Colorado applicants.
TRAVEL REQUIREMENTS:
20%-50%
WHAT TAKEDA CAN OFFER YOU:
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