Senior Manager Clinical Supply

GQR; San Francisco (CA); Hybrid; USD 180,000 - 240,000; Full time

Job summary

GQR is seeking a Senior Manager, Clinical Supplies Planning & Logistics to lead global IP forecasting, packaging, labeling, and distribution for Phase I-III studies. You will build study-level demand forecasts, select and manage CMOs, and design compliant packaging strategies worldwide.

The role requires 10+ years in biotech/pharma with 6+ years in clinical supplies, strong knowledge of cGMP/GCP/GDP, IRT/RTSM expertise, and vendor-management finesse.

Qualifications

• Ten-plus years in biotech/pharma with at least six years in clinical supplies.
• Experience managing global, blinded, small-molecule trials.
• Strong grasp of regulatory requirements (cGMP/GCP/GDP).

Responsibilities

• Build study-level demand forecasts and supply plans.
• Select, contract, and manage CMOs, depots, and logistics vendors.
• Design compliant packaging/labeling and blinding strategies worldwide.
• Lead IRT/RTSM implementation and lifecycle support.
• Author IP documents, train sites, and ensure inspection readiness.
• Oversee import/export, temperature excursions, and drug accountability.
• Partner across Clinical Ops, QA, CMC, and Regulatory to meet timeline and budget goals.

Skills

Leadership

Vendor management

IRT RTSM

Regulatory compliance

Cross-functional

Biotech domain

Education

Bachelor's degree in a related field

Job description

Senior Manager, Clinical Supplies Planning & Logistics

Our client - an innovative, publicly traded biotech with a first-in-class small-molecule pipeline - is searching for a seasoned CSPL leader to run global IP forecasting, packaging, labeling, and distribution for Phase I-III studies.

What You’ll Do

• Build study-level demand forecasts and supply plans.
• Select, contract, and manage CMOs, depots, and logistics vendors.
• Design compliant packaging/labeling and blinding strategies worldwide.
• Lead IRT/RTSM implementation and life-cycle support.
• Author IP documents, train sites, and ensure inspection readiness.
• Oversee import/export, temperature excursions, and drug accountability.
• Partner across Clinical Ops, QA, CMC, and Regulatory to meet timeline and budget goals.

What We’re Looking For

• B.S. or higher and 10+ years in biotech/pharma—6+ years specific to clinical supplies.
• Track record managing global, blinded, small-molecule trials.
• Strong grasp of cGMP/GCP/GDP and regional import/export rules.
• IRT/RTSM expertise and vendor-management finesse.
• Ability to thrive in fast-paced, cross-functional, partly remote teams.