Collaborates closely with global medical affairs team to ensure quality and timely medical contribution for key strategic submissions such as new applications, renewals, variations, etc.
Contributes to the creation of medical documents dedicated to Health Authorities and other national authorities.
Conducts rigorous analysis of medical/scientific data and participates in the elaboration and/or the evaluation of their publication.
Presents and drives the preparation for clinically driven topics for assigned non-core CHC portfolio in front of Governance Committees
Monitors medical news and publications, shares key learnings/alerts to global medical affairs and maintenance team
Facilitates internal medical trainings on CHC-relevant therapeutic areas and disease pathologies.
Reviews and approves promotional and non-promotional communication materials for non-core CHC portfolio.
Provides scientific monitoring oversight activities of medical vendors
Proactively identifies and communicates to higher management potential medical risks and options for issue resolution (e.g.: maintenance issues, submissions, etc.)
Follows CHC governance, ensuring Sanofi/industry standards are maintained at all times while looking for opportunities to streamline processes in the future
Ensures ethics, transparency, quality, and compliance of all medical activities (internal policy, procedures)
Qualification & Experience
Medical or Pharmacy Degree. Scientific/health related degree (PhD, Phar.D.) is acceptable if supported by good experience.
At least 3 years of relevant work experience in Pharmaceutical Industry and/or in Consumer Healthcare is a real asset