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Best fit for candidates who like regulated supply work inside big pharma, not pure commercial logistics. Comfort with process rigor, India-based study support, and occasional pressure from enrollment spikes matters more than flashy product marketing experience.
As a Clinical Trial Supply Manager at Novartis in India, a typical day centers on planning and releasing investigational product for global or regional studies: forecasting demand, coordinating packaging/labeling and depot shipments, tracking inventory and expiry, resolving site supply issues, and aligning with clinical ops, quality, and logistics so kits arrive on time without overstock or stockouts.
Prioritize clinical trial supply planning, cold-chain and controlled-substance handling basics, IRT inventory, deviation/CAPA literacy, and stakeholder communication. Build fluency in forecasting tools and GxP documentation; formal certs are optional here with no listed cost data.
Study drug availability: forecasts, packaging/labeling readiness, shipments to depots and sites, and issue resolution under GxP.
Listed as non-remote for India; expect on-site or hybrid norms set by the local Novartis site.
Clinical supply, pharmacy, QA, or pharma logistics experience with inventory systems and cross-functional coordination.
Website: novartis.com
Novartis AG is a Swiss multinational pharmaceutical corporation based in Basel, Switzerland. Novartis is one of the largest pharmaceutical companies in the world and was the eighth largest by revenue in 2024.
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Clinical Trial Supply Manager at Novartis in India About This Position The Clinical Trial Supply Manager (CTSM) is responsible for defining and executing an optimal clinical trial supply strategy, ensuring effective risk management to maintain supply continuity for patients. The CTSM serves as the single point of contact within the Global Clinical Supply team at the trial level, collaborating with the respective core CTT (Clinical Trial Team) or sub-team they represent. Day-to-Day Responsibilities Develop and implement an effective clinical supply strategy for assigned trials. Manage risks associated with supply chain disruptions to ensure patient continuity of care. Act as the primary liaison between the Global Clinical Supply team and local CTTs/sub-teams. Ensure compliance with all regulatory requirements related to clinical trial supplies. What You Bring A strong background in clinical research or supply chain management. Exposure to global clinical trials, particularly in the pharmaceutical industry. Excellent communication and interpersonal skills for effective collaboration with cross-functional teams. A proven track record of managing complex projects and ensuring timely delivery. More About Novartis Novartis is a global leader in the biopharmaceutical industry, committed to improving access to healthcare solutions. As part of our team, you will contribute to groundbreaking research and development that impacts millions of lives worldwide. Apply Today To apply, complete your application directly on this page, or you'll be redirected to the employer's application platform to finish submitting there.
Generated for personal interview prep · 2026-08-17 UTC · getajob.ai