Clinical Supplies Coordinator
Compensation
$60K - 80K a year
Responsibilities
Monitor and assess temperature data for clinical trial shipments, manage documentation, partner with QA to resolve excursions, and support clinical supply operations.
Requirements
1-3 years pharmaceutical supply chain or cold chain experience, understanding of GMP/GDP, experience with IRT systems preferred, and bachelor's degree in relevant field.
Full Description
Job Description: We are seeking a detail-oriented and collaborative Clinical Supplies Associate, supporting temperature excursion (TE) management and broader clinical supply activities. This role is critical to ensuring the integrity and compliance of clinical trial materials across the supply chain. Key Responsibilities: • Pharmaceutical supply chain or cold chain management • Monitor & assess temperature data for clinical trial shipments • Partner with QA to resolve excursions and ensure compliance • Manage documentation in IRT systems and eTMF • Support broader clinical supply operations (product destruction, study closeout, etc.) Education: • 1–3 years’ experience in pharmaceutical supply chain, cold chain, or stability management • Solid understanding of GMP and GDP standards • Experience with IRT systems and clinical documentation tools (preferred) • Bachelor's degree in Supply Chain Management, Life Sciences, Pharmacy, or related field
This job posting was last updated on 10/19/2025
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