Sr Clinical Supply Operations Specialist

Role: The Sr. Clinical Supply Operations Specialist supports clinical drug supply and logistics for complex studies across multiple therapeutic areas, focusing on inventory management, shipment coordination, and compliance with regulatory standards. Responsibilities include supply planning, inventory reconciliation, shipment and temperature excursion management, documentation for regulatory filings, vendor coordination, and budget forecasting. The role may lead short-term projects and participates in continuous improvement initiatives. Requirements: BS/BA in a related field with at least 3+ years of experience in clinical supplies, QA/regulatory, supply chain, or biopharma research/operations. Skills include knowledge of clinical development processes, GCP/ICH guidelines, proficiency in MS Office, problem-solving, and communication. Preferred qualifications include experience with biologics, precision medicine, or manufacturing in a clinical trial context. High-value specifics: supporting highly complex studies with international logistics, compliance with GxP standards, and involvement in regulatory documentation. Location: Warren, NJ or Armonk, NY, with up to 25% travel. The position involves cross-functional collaboration, adherence to regulatory policies, and working within a fast-paced, science-driven environment.