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Global Medical Expert

5+ years
₹25–35 LPA
10 May 23, 2025
Job Description
Job Type: Education: MBBS/MD Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Global Medical Expert
Location: Hyderabad, India
Salary Estimate: ₹25–35 LPA (based on industry standards and role seniority)


About the Role:

Join Sanofi and become a driving force in transforming healthcare through advanced scientific innovation and global medical support. As a Global Medical Expert, you will shape the future of chronic disease management, spanning diabetes, cardiovascular conditions, and more, while collaborating with international teams to ensure high-quality, regulatory-compliant medical documentation and assessments.


Key Responsibilities:

Medical Content & Documentation:

  • Provide medical assessments for documents like PBRERs, ACOs, DSURs, Clinical Overviews, and labeling.

  • Draft extended study synopses in collaboration with RWE experts.

  • Write clinical sections of CTDs and briefing packages.

  • Approve compassionate use requests for life-threatening conditions.

  • Ensure timely delivery of high-standard medical content.

Strategic & Regulatory Insight:

  • Offer medical input into global dossiers and product strategies.

  • Ensure compliance with regulatory standards across global regions (FDA, EU, etc.).

  • Maintain up-to-date knowledge in therapeutic areas such as cardiovascular, diabetes, oncology, etc.

Stakeholder Collaboration:

  • Partner with Medical Leads, Regulatory Affairs, Pharmacovigilance, and vendors.

  • Interact with internal departments to align deliverables with business needs.

  • Assist in refining medical regulatory strategies and enhancing content quality based on feedback.

Team Contribution:

  • Guide and mentor medical regulatory writers across experience levels.

  • Share expertise and support ongoing knowledge development within the team.


Candidate Profile:

Experience Required:

  • 5+ years in international pharmaceutical environments in Medical Affairs, Clinical Development, or Pharmacovigilance.

  • Hands-on experience in at least one key therapeutic area (cardiovascular, diabetes, oncology, etc.).

Education:

  • MBBS or MD degree (mandatory).

Skills:

  • Soft: Strong communication, stakeholder management, and team collaboration.

  • Technical: Expertise in medical writing, editing, risk and time management, medical regulatory processes.

  • Language: Proficient in English (written and spoken).


Why Join Sanofi?

  • Be part of a company accelerating innovation using AI and digital tools.

  • Collaborate with a global team striving for better healthcare outcomes.

  • Experience a culture that values diversity, equity, and inclusion.