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Sanofi, a global healthcare leader, is hiring for R&D Global Supply Study Support in Hyderabad, India. This role offers the opportunity to work in clinical supply chain operations (CSCO), ensuring investigational medical products (IMPs) are delivered to patients worldwide for clinical trials.
If you are passionate about clinical research, regulatory compliance, and pharmaceutical supply chain management, this is your chance to be part of a global, multicultural team that shapes the future of medicine.
🔑 Key Responsibilities
As part of the Global Supply Study Support (GSSS) team, you will:
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- Manage IMP transfers to depots and maintain stock trackers in Sanofi’s systems.
- Monitor and resolve IRT interface failures in supply tools.
- Perform IMP reconciliation, returns, and destruction activities.
- Archive IMP-related documentation in eTMF to ensure inspection readiness.
- Track shipments, monitor stock levels, and support regulatory inspection preparation.
- Manage service provider purchase orders, invoices, and financial compliance.
- Collaborate with Clinical Supply Chain Study Leaders (CSC SL) across the USA, France, and China.
🎓 Qualifications & Skills
- Education: Bachelor’s degree (Science/Pharma preferred). Advanced degree is a plus.
- Experience: Minimum 2 years in pharmaceutical production, supply chain, quality, or clinical trials.
- Knowledge: Good Clinical Practice (GCP) and Good Manufacturing Practice (GMP).
- Skills:
- Strong organizational and multitasking ability
- Effective verbal and written communication
- Proficiency in MS Office, IRT, ERP, Veeva, and digital trial tools
- Ability to adapt in a global, multicultural environment
🌍 Why Join Sanofi?
- Work with a leading global biopharma company.
- Exposure to international clinical supply chain operations.
- Opportunity to advance in regulatory and clinical operations.
- Inclusive workplace with strong focus on Diversity, Equity, and Inclusion (DEI).
📌 How to Apply

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