×
Register Here to Apply for Jobs or Post Jobs. X

Associate Director, Global Clinical Supply Chain Operations

Job in Lexington, Middlesex County, Massachusetts, 02173, USA
Listing for: Takeda
Full Time position
Listed on 2026-01-19
Job specializations:
  • Healthcare
    Healthcare Administration, Healthcare Management
Job Description & How to Apply Below

Associate Director, Global Clinical Supply Chain Operations

Join Takeda in Cambridge, MA as an Associate Director in Global Clinical Supply Chain Operations. This patient‑focused, innovation‑driven role empowers you to shine while supporting global R&D clinical trials.

POSITION OBJECTIVES
  • Lead and execute GCSC activities worldwide under the direction of the GCSC Director.
  • Manage Clinical Supply project delivery for Takeda Global R&D Clinical Trials and other research needs.
  • Coordinate, procure and manage drug product supply, packaging, labeling, distribution, return, reconciliation, and destruction activities of clinical trial material.
  • Develop and communicate clinical supply project budgets and plans to ensure all project objectives are met timely and compliant.
  • Provide expertise, collaborate internally, and lead Global Clinical Supply Chain group initiatives including active participation of the study oversight process.
POSITION

ACCOUNTABILITIES
  • Interpret clinical trial drug requests and clinical protocols with GCSC Planning to develop supply packaging strategies, timelines, and budgets.
  • Utilize the Smart Supplies Database (PMD) for clinical labeling approval and manage inventory, shipments, and drug return activities.
  • Provide input into Interactive Response Technology (IRT) design for randomization and supply drug to depots and sites.
  • Interface with QA/QP personnel to facilitate expeditious release of clinical trial material for shipment to sites.
  • Interface with Pharmaceutical Sciences group to ensure supplies are supported with stability programs and expiry dating.
  • Collaborate with Logistics to plan, document, and facilitate global cross‑border supply strategies for controlled substances and regulatory requirements.
  • Manage and troubleshoot shipment requests, drug returns, Smart Supplies, and IRT processes with GCSC Specialists and maintain project documentation.
  • Oversee primary and secondary packaging, labeling, testing, distribution, return drug management activities with service providers per approved budget.
  • Key interface with Clinical Operations and Regulatory Affairs on information required for Health Authority Submissions.
  • Evaluate and propose system improvements and technology enhancements/opportunities.
  • Manage external consultants and third‑party vendors to ensure timely and quality delivery of CTM that meets study protocol, regulatory, and budgetary requirements.
  • Accountable for amending budgets through defined change management processes and manage finance activities with clinical team.
  • Coach and mentor less experienced staff.
  • Implement improvement opportunities and business processes related to the Clinical Supplies Team.
  • Manage specialized or high‑profile projects and serve as backup to the director when needed.
EDUCATION, BEHAVIORAL COMPETENCIES AND SKILLS
  • Degree in Pharmacy, other scientific/technical degree, or significant job‑related experience.
  • Minimum of 8 years relevant Pharmaceutical Industry and/or Contract/Service Provider experience preferred.
  • Experience with oncology a plus.
  • Strong understanding of cGMP requirements.
  • Proficiency in computer software applicable to IRT, Excel and MS Project or equivalent project management software a plus.

This position is currently classified as “hybrid” in accordance with Takeda’s Hybrid and Remote Work policy.

Location

Lexington, MA

Takeda Compensation and Benefits Summary

U.S. Base Salary Range: $ - $
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.
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…

Position Requirements
10+ Years work experience
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)

Job Posting Language
Employment Category
Education (minimum level)
Filters
Education Level
Experience Level (years)
Posted in last:
Salary