Role Summary:
The Associate Director, Clinical Supply Chain will lead the planning and execution of global clinical supply activities at Triveni, ensuring uninterrupted drug supply for early-stage clinical programs. Reporting to the Sr. Director of Technical Operations, the role covers end-to-end supply chain management, including packaging, labeling, distribution, IRT system oversight, and cross-functional collaboration with clinical, regulatory, and manufacturing teams.
Key Responsibilities:
- Manage global clinical supply planning, inventory, shipping, and vendor oversight
- Oversee packaging, labeling, and distribution in collaboration with CMC
- Develop global distribution plans and manage IRT systems
- Ensure compliance with cGMP, regulatory guidelines, and internal SOPs
- Author or review supply-related documentation (e.g., label text, IBs, protocols)
- Build and optimize internal supply chain infrastructure and processes
Qualifications:
- 5+ years in clinical supply chain (preferably with biologics)
- Experience with global trials, CDMOs, CROs, and IRT systems
- Strong knowledge of cGMP and regulatory standards
- Proven cross-functional collaboration skills (CMC, Regulatory, Clinical Ops)
- Background in biotech/pharma start-up environments preferred
- Strong leadership, communication, and organizational abilities
- BS or MS in a relevant scientific or technical field
Job sourced from Triveni Bio.