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Senior Manager, Clinical Supply Chain

Sumitomo Pharma America

Job Location:

Marlborough, NH - USA

Hourly Salary: USD 100 - 103

Posted: 8 September 2026 (18 hours ago)

Application Deadline: 6 December 2026

Vacancies: 1 Vacancy

Job Summary

Job Title: Senior Manager Clinical Supply Chain
Location: Marlborough MA-01752
Duation:12 Months
Pay Rate:$100-$103 on W2/hourly

JOB DESCRIPTION

Responsible for managing drug supply planning inventory control and distribution activities including label/pack scheduling issue resolution change implementation vendor oversight and scope review related to clinical supplies on multiple clinical programs.
In addition working closely with CClient Regulatory Affairs Quality Assurance Clinical Operations and /or SMPA external partners and CMOs as needed building strong working relationships support study project teams and ensure timely Investigational Product (IP) for clinical trials.

Skills:
Lead and manage end-to-end Clinical Supply Chain activities (planning packaging and labeling distribution returns and destruction) for assigned clinical programs in early and late phases.
Develop and manage supply forecasts supply plans and timelines in collaboration with Clinical and CClient.
Manage IP inventory levels at the depots and clinical sites; coordinate the inventory from manufacturer to depot or clinical sites.
Design and/or review label text to meet product requirements and ensure compliance with US and international regulations.
Ensures effective management of IP based on study timing and in accordance with clinical protocols cGMP GCP ICH FDA and other applicable international federal and/or local regulations.
Collaborate closely with Clinical Operations CClient Regulatory Affairs QA and PDM to ensure advancement of clinical programs; ensure supplies readiness.
Manage clinical supply and logistics and resolve issues such as shipment delays temperature excursions import/export; work closely internal Trade Compliance & Logistics team.
Demonstrates a solid understanding of clinical study design (randomized blinded open label etc.) and execution.
Manage assign clinical trial contracts purchase orders including invoices and budget for clinical supply vendor; participate in CSC budget and forecast planning.
Represent Clinical Supply Chain function at clinical trial meetings; communicate plan and timelines to internal and external customers and partners.

Education:
BS/BA degree (Masters preferred) in life sciences or business major or equivalent required.
Minimum 5-7 years in life sciences industry related experience including Project Management Pharmaceutical Development Clinical Supply Management and/or Clinical Trials Coordination.
At least 3 years in Clinical Supplies Management.
Proficient knowledge of Microsoft Excel PowerPoint and Project software required.
APICS certification (CPIM CLTD CSCP) preferred.