Job Title:
Medical Affairs Manager – CHC Portfolio
Company:
Sanofi
Location:
Hyderabad, India
Job Type:
Full-time, Permanent
Main Responsibilities:
1. Regulatory & Scientific Contributions:
Collaborate with global medical affairs teams to contribute to strategic regulatory submissions including new applications, renewals, and variations.
Support creation of medical documentation for Health Authorities and other national bodies.
Analyze medical/scientific data for submission and publication purposes.
Lead preparation and presentation of clinically-driven topics related to the non-core CHC portfolio for Governance Committees.
2. Scientific Communication & Monitoring:
Track medical news and relevant publications; extract insights and share updates with medical affairs and maintenance teams.
Facilitate internal medical trainings on CHC-relevant therapeutic areas and disease pathologies.
Review and approve promotional and non-promotional content related to the non-core CHC portfolio.
3. Compliance & Vendor Oversight:
Supervise scientific oversight of external medical vendors.
Identify and escalate potential medical risks, suggesting solutions to management (e.g., maintenance issues, submission delays).
Adhere to CHC governance and ensure that all processes follow Sanofi/industry standards.
Ensure compliance, ethics, transparency, and quality in all medical affairs activities.
About You:
Education:
Medical (MBBS/MD) or Pharmacy (BPharm/MPharm/PharmD) degree
PhD or other life science degrees accepted with relevant experience
Experience:
Minimum 3 years in the pharmaceutical or consumer healthcare industry
Experience in global or regional roles is a plus
Technical/scientific writing experience for Health Authorities or publications preferred
Soft Skills:
Strong scientific analysis and data interpretation skills
Ability to work under tight deadlines and handle a high workload
Effective networking and collaboration across teams and functions
Organized, detail-oriented, and proactive
Flexible and adaptable to evolving priorities and timelines
Able to problem-solve, evaluate risks, and propose solutions
Strong team player in a multi-disciplinary and global setup
Technical Skills:
Proficiency in technical/scientific writing for submissions and publications
Knowledge of international regulatory requirements, guidelines, and best practices
Proficient in Microsoft Office Suite
Languages:
Fluent in English (spoken and written)
Additional languages are a plus
Sanofi Commitment to Diversity:
At Sanofi, diversity fuels our progress. We are proud to be an equal opportunity employer. All individuals, regardless of background, are encouraged to apply.
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Canada |Quebec :
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Japan | Saitama |Tokyo :
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