Clinical Supply Associate
About The Position
Join Pharmaceutical Technology & Development (PT&D) and help turn innovative science into medicines for millions. As a Clinical Supply Associate, you’ll support Clinical Supply Chain Management by delivering clinical materials and critical information. You will help meet trial demand in a fast-paced, global environment committed to achieving goals. This role offers early leadership exposure, enterprise acuity, and the chance to become a super-user and lead improvement initiatives within your first year. What you’ll do: Temperature excursion management: Lead assessments impacting clinical trial material (over 50% of the role). Quality and compliance: Coordinate product quality complaints, GxP deviations, and ensure documentation is inspection-ready to international GMP standards. Digital systems: Support electronic archiving and quality control; perform user acceptance testing for digital tools. Supply chain support: Use clinical supply systems to enable agile ways of working and visual management. Continuous improvement: Drive problem-solving, global standardization, and process confirmation. Join an Operations team shaped by growth, new products, and continuous evolution. Influence how we design supply chains, embed a Lean perspective, and lead on sustainability. In our agile philosophy, you’ll speak up, improve processes, and implement faster—working openly as a team to solve problems and advance together. Ready to break new ground and leave a collective legacy? Apply now.
Requirements
- Education: Bachelor’s or Master’s in a scientific subject area or supply chain leadership.
- Experience: 1+ year of GxP operational experience.
- Skills: Excellent communication and numeracy; highly organized with strong digital proficiency; effectively engaged with GenAI; customer/patient-focused; team-oriented with a quality perspective; comfortable in a high-paced, agile setting; able to zoom out to the big picture while handling detail.
Responsibilities
- Temperature excursion management: Lead assessments impacting clinical trial material (over 50% of the role).
- Quality and compliance: Coordinate product quality complaints, GxP deviations, and ensure documentation is inspection-ready to international GMP standards.
- Digital systems: Support electronic archiving and quality control; perform user acceptance testing for digital tools.
- Supply chain support: Use clinical supply systems to enable agile ways of working and visual management.
- Continuous improvement: Drive problem-solving, global standardization, and process confirmation.
Benefits
- qualified retirement programs
- paid time off (i.e., vacation, holiday, and leaves)
- health, dental, and vision coverage
- opportunity to receive short-term incentive bonuses
- equity-based awards for salaried roles
- commissions for sales roles
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Number of Employees
5,001-10,000 employees
