Senior Director, Clinical Safety MD
Company: Daiichi Sankyo
Location: Basking Ridge
Posted on: January 25, 2026
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Job Description:
Job Description Job Title: Senior Director, Clinical Safety MD
Job Requisition ID: 718 Posting Start Date: 1/15/26 At Daiichi
Sankyo, we are united by a single purpose, to improve lives around
the world through innovative medicines. With a legacy of innovation
since 1899, a presence in more than 30 countries, and more than
19,000 employees, we are advancing breakthrough therapies in
oncology, cardiovascular disease, rare diseases, and immune
disorders. Guided by our 2030 vision to "be an innovative global
healthcare company contributing to the sustainable development of
society", we are shaping a healthier, more hopeful future for
patients, their families, and society. Job Summary The Sr.
Director, Clinical Safety, will lead the development and
implementation of integrated project/product risk management
strategies aimed at achieving the optimum benefit-risk for
Development Sankyo's development compounds through the Safety
Management Team framework. This individual will use strong
leadership and communication skills to successfully coordinate
resources and ensure effective collaboration across development
functions and sites. The individual assuming this role may function
as a key member of the Global Product Team in collaboration with
Clinical Development, Regulatory, Project Management,
Biostatistics, Pharmacology, and other departments to strategically
manage benefit-risk throughout the lifecycle of the drug. Specific
responsibilities will vary depending on the stage of development of
assigned projects (i.e., Phase I through commercialization). Job
Description Responsibilities Responsibilities: Depending on the
status of development of the compound, lead and
medical-scientifically direct a team of physicians and scientists
responsible for a compound/product including project-specific
training and coaching of team members and review of team output
cross-functionally. Effectively represent the CSPV on the Global
Product Team or other cross-functional teams providing the safety
leadership and serving as the primary point of contact. Review and
analyze data from clinical trials, post-marketing and other
relevant sources for the prompt identification of safety signals.
Lead internal and external (especially regulatory, but also expert
advisory) interactions to ensure quality outcomes in the risk
evaluation and management of assigned projects/products. Define and
implement strategies and action plans for identifying and managing
risks throughout the product life cycle. Effectively coordinate and
manage available resources in developing and delivering
high-quality safety evaluation related documents/deliverables on
time. Coordinate and participate actively in safety-related
regulatory interactions (e.g., regulatory meetings, post-approval
commitments). Responsibilities Continued Qualifications
Qualifications: Successful candidates will be able to meet the
qualifications below with or without a reasonable accommodation.
Education Qualifications (from an accredited college or university)
MD is required (board certification or eligibility) Experience
Qualifications: 6 or more years of experience in the pharmaceutical
industry, regulatory agency or academia, with exposure to drug
development, clinical pharmacology, and/or epidemiology. Expertise
in oncology highly preferred. Travel: Some travel both domestic and
global will be required. Additional Information Daiichi Sankyo,
Inc. is an equal opportunity/affirmative action employer. Qualified
applicants will receive consideration for employment without regard
to sex, gender identity, sexual orientation, race, color, religion,
national origin, disability, protected veteran status, age, or any
other characteristic protected by law. Salary Range: USD$275,250.00
- USD$458,750.00 Download Our Benefits Summary PDF
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Keywords: Daiichi Sankyo, Irvington , Senior Director, Clinical Safety MD, Science, Research & Development , Basking Ridge, New Jersey