Lead a team of trial supply professionals and establish clear priorities, accountabilities, performance expectations, and ways of working across an assigned portfolio of clinical trials.
Compensation
The anticipated base pay range for this position is: €97,900.00 - €168,360.00
Responsibilities
Lead a team of trial supply professionals and establish clear priorities, accountabilities, performance expectations, and ways of working across an assigned portfolio of clinical trials.
Translate Trial Supply Delivery strategy and functional objectives into portfolio plans that align with Clinical Supply Chain priorities, Global Clinical Operations needs, and clinical development milestones.
Ensure end-to-end trial supply setup and execution to deliver clinical supplies to depots and investigative sites when and where needed to support uninterrupted patient dosing.
Provide portfolio-level oversight of startup readiness, inventory health, site delivery, patient supply continuity, issue resolution, and inspection readiness using defined metrics and performance reviews.
Serve as the primary escalation point for complex trial supply execution issues and partner with Global Clinical Operations, Quality, E2E Planning, Manufacturing, Logistics, Procurement, and external service providers to drive resolution.
Requirements
Bachelor's degree in supply chain, engineering, logistics, life sciences, pharmaceutical sciences, business, operations management, or a related discipline
Lead a team of trial supply professionals and oversee end-to-end clinical trial supply execution.
Locations (3)
Horsham, Pennsylvania, United States
Titusville, New Jersey, United States
Belgium
Compensation
The anticipated base pay range for this position is : $140,000.00 - $241,500.00
Responsibilities
Lead a team of trial supply professionals and establish clear priorities, accountabilities, performance expectations, and ways of working across an assigned portfolio of clinical trials.
Translate Trial Supply Delivery strategy and functional objectives into portfolio plans that align with Clinical Supply Chain priorities, Global Clinical Operations needs, and clinical development milestones.
Associate Director, Trial Supply Execution
6084-Janssen Research & Development Legal Entity · Posted Nov 5, 2026
Lead a team of trial supply professionals and establish clear priorities, accountabilities, performance expectations, and ways of working across an assigned portfolio of clinical trials.
Locations (2)
Horsham, Pennsylvania, United States
Titusville, New Jersey, United States
Compensation
The anticipated base pay range for this position is : $140,000.00 - $241,500.00
Responsibilities
Lead a team of trial supply professionals and establish clear priorities, accountabilities, performance expectations, and ways of working across an assigned portfolio of clinical trials.
Translate Trial Supply Delivery strategy and functional objectives into portfolio plans that align with Clinical Supply Chain priorities, Global Clinical Operations needs, and clinical development milestones.
Ensure end-to-end trial supply setup and execution to deliver clinical supplies to depots and investigative sites when and where needed to support uninterrupted patient dosing.
Associate Director, Trial Supply Execution
6084-Janssen Research & Development Legal Entity · Posted Nov 5, 2026
The Associate Director, Trial Supply Delivery is accountable for leading a team of trial supply professionals responsible for the end-to-end setup and execution of clinical trial supply activities from study initiation through Last Patient Dosed.
Locations (2)
Beerse, Antwerp, Belgium
United States
Compensation
The anticipated base pay range for this position is €97,900.00 - €168,360.00
Responsibilities
Lead a team of trial supply professionals and establish clear priorities, accountabilities, performance expectations, and ways of working across an assigned portfolio of clinical trials.
Translate Trial Supply Delivery strategy and functional objectives into portfolio plans that align with Clinical Supply Chain priorities, Global Clinical Operations needs, and clinical development milestones.
Ensure end-to-end trial supply setup and execution to deliver clinical supplies to depots and investigative sites when and where needed to support uninterrupted patient dosing.
Provide portfolio-level oversight of startup readiness, inventory health, site delivery, patient supply continuity, issue resolution, and inspection readiness using defined metrics and performance reviews.
Ensure end-to-end trial supply setup and execution to deliver clinical supplies to depots and investigative sites when and where needed to support uninterrupted patient dosing.
Provide portfolio-level oversight of startup readiness, inventory health, site delivery, patient supply continuity, issue resolution, and inspection readiness using defined metrics and performance reviews.
Serve as the primary escalation point for complex trial supply execution issues and partner with Global Clinical Operations, Quality, E2E Planning, Manufacturing, Logistics, Procurement, and external service providers to drive resolution.
Requirements
Bachelor's degree in supply chain, engineering, logistics, life sciences, pharmaceutical sciences, business, operations management, or a related discipline
Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year
Holiday pay, including Floating Holidays –13 days per calendar year
Work, Personal and Family Time - up to 40 hours per calendar year
Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
Provide portfolio-level oversight of startup readiness, inventory health, site delivery, patient supply continuity, issue resolution, and inspection readiness using defined metrics and performance reviews.
Serve as the primary escalation point for complex trial supply execution issues and partner with Global Clinical Operations, Quality, E2E Planning, Manufacturing, Logistics, Procurement, and external service providers to drive resolution.
Requirements
Bachelor's degree in supply chain, engineering, logistics, life sciences, pharmaceutical sciences, business, operations management, or a related discipline
Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year
Holiday pay, including Floating Holidays –13 days per calendar year
Work, Personal and Family Time - up to 40 hours per calendar year
Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
Serve as the primary escalation point for complex trial supply execution issues and partner with Global Clinical Operations, Quality, E2E Planning, Manufacturing, Logistics, Procurement, and external service providers to drive resolution.