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Clinical Supply Chain Project Leader

Job in Cambridge, Middlesex County, Massachusetts, 02140, USA
Listing for: Eacademy Sanofi
Full Time position
Listed on 2026-07-13
Job specializations:
  • Business
    Operations Management, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 120000 - 150000 USD Yearly USD 120000.00 150000.00 YEAR
Job Description & How to Apply Below

Job Title
:
Clinical Supply Chain Project Leader

Location
:
Cambridge, MA

About the Job

The Clinical Supply Chain Project Leader (CSC-PL) is accountable for IMP supply with respect to timelines, quality and budget for a given project.

The CSC-PL is responsible to:

  • Defines and implements the CSC Strategy at project level.
  • Oversees study management activities ensuring adherence to plan.
  • Represents CSC at project level.

The CSC-PL will also ensure clear, concise, consistent, and timely communication with stakeholders and act as a change agent through the leadership of global initiatives targeting process improvement and engaging all partners throughout the clinical supply chain.

Responsibilities CSC Strategy & Implementation
  • Define and implement clinical supply chain strategy aligned with CSC KPIs and project objectives.
  • Assess study design feasibility ( card, abbreviated protocol stages) and optimize project delivery.
  • Influence label & pack outsourcing and distribution network strategy decisions.
  • Monitor supply chain performance (cost, lead times, quality) using KPIs and digital tools.
  • Drive continuous improvement and innovation across clinical supply chain operations.
Study Management Oversight
  • Lead CSC-Study Leaders and oversee all operational activities ensuring compliance with GCP/GMP standards.
  • Ensure CSC strategy harmonization across multiple trials with adherence to timelines and budget.
  • Monitor plan execution, identify risks, and implement mitigation plans.
  • Identify opportunities to streamline processes and reduce lead times and costs.
  • Serve as primary point of contact for project team and coordinate PAI preparation.
CSC Representation & Stakeholder Communication
  • Provide CSC expertise and contribute to project decision‑making in project meetings.
  • Escalate IMP/device/AXMP/comparator issues and propose mitigation strategies.
  • Interact with GPH, CMC leaders, and clinical leaders to integrate CSC requirements into project strategy.
  • Report progress and issues to CSC Leadership Team.
  • Facilitate knowledge sharing and provide feedback on contractor performance.
About You Education
  • Bachelor’s degree with at least 5+ years OR Master’s degree with at least 3+ years preferably in health sciences or related disciplines (engineering, pharmacy, chemistry, biology, etc.).
Experience & Technical Skills
  • Experience in pharmaceutical industry, preferably within clinical supply chain, clinical operations, or manufacturing environments.
  • Project management experience.
Preferred Qualifications
  • Experience with GxP regulations and IMP requirements.
  • Any experience with N-SIDE forecasting systems, IRT systems preferred.
  • Risk management experience.
Soft Skills
  • Demonstrated leadership experience in engaging and ensuring collaboration across different functions.
  • Excellent workload prioritization within a dynamic, timeline‑driven, culturally diverse organization.
  • Advanced organizational, planning, and prioritization skills with effective problem‑solving and decision‑making abilities.
  • Excellent communication (written and oral), negotiation, and influencing skills.
  • Ability to build and maintain efficient professional relationships with partners and stakeholders.
  • Experience operating in cross‑cultural and complex organizational matrices.
  • Self‑driven with effective time management skills.
Why Choose Us
  • Bring the miracles of science to life alongside a supportive, future‑focused team.
  • Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
  • Enjoy a thoughtful, well‑crafted rewards package that recognizes your contribution and amplifies your impact.
  • Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high‑quality healthcare, prevention and wellness programs and at least 14 weeks’ gender‑neutral parental leave.
  • Be part of a pioneering biopharma company that engages patients early in drug development and uses their insights to design studies that reflect real‑world needs.
  • Help improve the lives of millions of people globally by making drug development quicker and more effective.
  • Work at the forefront of drug discovery,…
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