Senior Manager, Clinical Supply Chain Management

Scorpion Therapeutics; Lexington (MA); On-site; USD 180,000 - 230,000; Full time

Job summary

Scorpion Therapeutics in Lexington, MA is seeking an Associate Director, Clinical Supply Chain Management to lead global clinical material strategy across studies.

You will oversee supply planning, vendor management, packaging/labeling, comparator sourcing, distribution, and study closeout, while building forecasts, budgets, and regulatory compliance. This onsite role requires 6+ years in biopharma clinical supply and strong cross-functional influence.

Qualifications

• BS/BA with 6+ years in clinical supply chain within biopharma.
• Experience managing multi-study programs and vendor oversight including packaging/labeling.

Responsibilities

• Oversee supply planning, vendor management, packaging, labeling, comparator sourcing, distribution and study closeout.
• Develop demand forecasts, manage budgets and ensure regulatory compliance.

Skills

Project management

Cross-functional collaboration

Regulatory awareness

Education

BS/BA in life sciences

Job description

Role

Associate Director, Clinical Supply Chain Management, responsible for strategic and operational leadership of global clinical supply for multiple studies across phases.

Objectives

ensure continuous trial material availability, mitigate risks, and align cross-functionally with Clinical Operations, Quality, Regulatory, and external partners.

Responsibilities

• oversee supply planning, vendor management, packaging, labeling, comparator sourcing, distribution, and study closeout;
• develop demand forecasts, manage budgets, and ensure compliance with regulatory standards.

Requirements

• BS/BA with 6+ years in clinical supply chain within biopharma, experience managing multi-study programs, and vendor oversight including packaging/labeling organizations.

High-Value

• experience supporting early to late-stage clinical development, global distribution expertise, knowledge of cGMP, GCP, GDP, and regulatory requirements across US, EU, and APAC;
• strong project management and cross-functional influence skills.

WorkSetup

based onsite in Lexington, MA; no travel specified.