Project Lead, CSO
Company: Daiichi Sankyo
Location: Basking Ridge
Posted on: March 18, 2026
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Job Description:
Job Description Job Title: Project Lead, CSO Job Requisition ID:
1204 Posting Start Date: 3/16/26 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 This position is responsible for enabling the
on-time delivery of clinical supplies across the DSI portfolio.
This role is primarily responsible for supporting CSO Project
Management Leads by developing and updating Study Supply Plans,
managing various work streams with key service providers and
working with internal departments to progress clinical supply
projects. Every effort has been made to identify the essential
functions of this position. However, it in no way states or implies
that these are the only duties you will be required to perform, nor
is it intended to be such a listing of the skills and abilities
required to do the job. The omission of specific statements of
duties does not exclude them from the position if the work is
similar, related, or is an essential function of the position.
Responsibilities Develops and updates Study Supply Plans in close
communication with CSO project Management Lead Responsible for the
Clinical Label Development process which includes creation of
master label text, translations, and label proofs. Manages the
packaging Batch Record review and approval process with Quality
Assurance and other CSO personnel. Works closely with Quality
Assurance to obtain temperature excursion disposition to update
impacted inventory in IRT and other related systems. Coordinates
authorized destruction of investigational products with approved
vendors and obtains required documentation. Vendor Management
–supports Person in Plant (PIP) activities when packaging
operations for DSI are in-process. Supports investigational product
distribution activities at the vendor, including generation of drug
orders, review of shipping documentation and obtaining approval to
ship Assists in the creation of SOP’s and work instructions
specific to CSO Supply Planning as requested. Responsible for
updating relevant Trial Master Files (TMF) with CSO-related
documents Supports the CSO Project Mgmt Lead in executing
additional operational and logistical duties as discussed and
agreed to by management Qualifications Education Qualifications
Bachelor's Degree Bachelor's degree in Science or related field.
Extensive experience will be considered in lieu of an advanced
degree required Experience Qualifications 7 or More Years of
related experience, including Project Management, Clinical Supply
Management, and/or Pharmaceutical Development. preferredOncology
experience preferred Creation of Supply Planning tools preferred
Travel Requirements Ability to travel up to 10% of the time.
Overnight / single-day travel will be required to go to outsourcing
vendors from time to time infrequently. 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$116,400.00
- USD$174,600.00 Download Our Benefits Summary PDF
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Keywords: Daiichi Sankyo, Irvington , Project Lead, CSO, Science, Research & Development , Basking Ridge, New Jersey