R&D eTMF Document Specialist and TMF Support Team Lead Roles in Clinical Research (Life Sciences, Pharmacy, Hyderabad) Sanofi in

Sanofi, a global leader in biopharmaceuticals, is hiring for two key roles at its Hyderabad R&D Hub: R&D eTMF Document Specialist and R&D TMF Support Team Lead. These positions are ideal for professionals with backgrounds in Life Sciences, Pharmacy, or related fields who are seeking to advance their careers in clinical research documentation and regulatory compliance.

The R&D eTMF Document Specialist will manage Trial Master File (TMF) documents across study, country, and site levels, ensuring completeness, accuracy, and inspection readiness. Responsibilities include performing metadata completion, quality control checks, supporting Veeva Vault eTMF users, coordinating document corrections, and assisting with audit and regulatory inspection preparation. Candidates should have a bachelor’s degree in Life Sciences or Pharmacy, experience in eTMF management or clinical documentation, strong knowledge of ICH-GCP and clinical trial processes, and excellent organizational and communication skills. Experience with Veeva Vault eTMF is preferred.

The TMF Support Team Lead will oversee the TMF Support Team, manage inspection readiness, QC, and TMF migration activities, and collaborate with global stakeholders. This role requires 3–5+ years of industry experience, including people management, a strong understanding of drug development and TMF regulations, and proven leadership and stakeholder engagement skills. Fluency in English is essential.

Salary ranges are ₹6,00,000 – ₹10,00,000 per annum for the Document Specialist and ₹15,00,000 – ₹25,00,000 per annum for the Team Lead, with additional benefits such as exposure to global clinical programs, career growth opportunities, and an inclusive work culture. The application deadline is February 4, 2026. Interested candidates should apply online via the provided links and ensure they meet the qualifications before submitting their applications.