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R&D Global Supply Study Support – Sanofi

Published on

Sanofi

B.Pharm, M.Pharm, Msc, BSc, B.Tech, M.Tech in Life Sciences, Pharmacy, Biotechnology, Chemistry, Supply Chain / Clinical Research Management

Hyderabad

2 years

Verified Job

Online Application
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Sanofi, a global healthcare leader, is hiring for the R&D Global Supply Study Support role in Hyderabad. This position is an exciting opportunity for professionals with experience in clinical trial supply chain management, investigational product (IMP) logistics, and regulatory compliance. If you are passionate about supporting global clinical studies and ensuring timely delivery of life-saving investigational medicines, this role offers a perfect platform to grow your career in pharmaceutical R&D operations.

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Key Responsibilities

As an R&D Global Supply Study Support professional at Sanofi, your core responsibilities will include:

Clinical Trial & Supply Knowledge

  • Understand clinical trial design, protocols, and regulatory requirements (GxP).
  • Gain expertise in patient randomization, dosing regimens, and cohort management.
  • Manage IMP logistics including kit types, shelf life, depot management, and reconciliation.

Level 1 Duties

  • Create and manage depot transfers in IRT and Sanofi supply tools.
  • Oversee IMP destruction, reconciliation, and discrepancy investigations.
  • Support supply planning and maintain global inventory tracking systems.
  • Archive IMP-related documents in eTMF to ensure inspection readiness.

Level 2 Duties

  • Monitor IMP and AxMP stock levels, alerting CSC SL on shortage risks.
  • Assist in shipment tracking and preparation of regulatory documents.
  • Manage service provider purchase orders, invoices, and financial compliance.
  • Support CSC SL in regulatory inspections and audit preparation.

Qualifications

To qualify for this opportunity, candidates should have:

  • Bachelor’s degree (science preferred); advanced degree is a plus.
  • Minimum 2 years of experience in pharmaceutical production, supply chain, quality, or clinical trials.
  • Knowledge of Good Clinical Practice (GCP) and Good Manufacturing Practice (GMP).
  • Strong organizational, multitasking, and communication skills.
  • Ability to work in global, multi-cultural teams with adaptability.
  • Proficiency in MS Office, IRT, ERP, Veeva, PowerBI, and other clinical trial tools.
  • Near-native fluency in English (written & spoken).

Benefits of Working with Sanofi

  • Opportunity to work with a global leader in healthcare and clinical research.
  • Exposure to international clinical supply chain operations.
  • Collaborative and inclusive work culture that promotes growth.
  • Competitive compensation and career advancement opportunities.
  • Be part of a team committed to delivering better medicines and outcomes worldwide.

How to Apply

Application Link

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R&D Global Supply Study Support – Sanofi
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PharmaBharat Editorial Team

The PharmaBharat Editorial Team, comprised of pharmaceutical industry experts with over 3 years of collective experience in research, regulatory affairs, and market analysis, delivers accurate and timely updates on trends, innovations, and career opportunities. Our content is rigorously vetted by professionals with advanced degrees in pharmacy and biotechnology, ensuring authoritative and trustworthy insights for job seekers in the pharmaceutical sector.

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