Associate Medical Director Hematology, US OBU Medical Affairs
About The Position
Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as an Associate Medical Director Hematology, US OBU Medical Affairs 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.
Requirements
- MD, Ph.D, or Pharm D degree
- Expert in managing and overseeing clinical trials, ensuring adherence to protocols and timelines
- Skilled in strategic planning and execution of complex clinical research projects
- Proficient in data analysis and interpretation, capable of making data-driven decisions
- Strong leadership skills, able to guide and motivate a team towards achieving research objectives
- Experienced in negotiation, able to effectively manage study costs and design
- Effective collaborator, adept at working with different stakeholders including external partners
- Experienced mentor, capable of fostering talent and encouraging professional growth within the team
Responsibilities
- Execution of the US medical strategy for CML and Ph+ ALL.
- Scientific engagement with healthcare professionals, investigators, and external experts.
- Cross-functional collaboration with Clinical Development, Commercial, Market Access, and Field Medical teams.
- Support of evidence generation initiatives, medical education programs, congress activities, publications, and advisory boards.
- Development and review of scientific materials to ensure accurate and compliant communication of clinical data.
- Ensure the organization is aware of and compliant with legislation and regulations
- Monitor and interpret regulatory developments and determine their impact on business operations
- Implement compliance programs and ensure regulatory reporting/documentation for internal and external audiences
- Gather, prepare, review, and approve regulatory compliance documents
- Lead functional teams or projects, providing guidance in complex situations
- Communicate with leadership and provide consultative expertise
Benefits
- 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
- well-being benefits
- up to 80 hours of sick time
- up to 120 hours of paid vacation
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
Ph.D. or professional degree
