Contribute to Clinical Development Plans (CDP), product value propositions (TVP), and market access strategies in collaboration with relevant functions.
Provide medical input and support across all activities related to clinical studies, including medical training, feasibility, data review, and stakeholder communications.
Oversee the medical review of clinical trial data, safety event assessments, and coding of events and drugs.
Develop and amend clinical protocols and informed consent documents.
Prepare and review key clinical documents, such as Clinical Study Reports, Investigator Brochures, and Clinical Trial Authorization dossiers.
Collaborate closely with internal and external stakeholders to ensure optimal study execution in compliance with GCP, laws, and SOPs.
Manage clinical scientists and collaborate with cross-functional teams including medical affairs, pharmacovigilance, biostatisticians, and CROs.

Job Requirements

Proven scientific and medical expertise with a track record in clinical development.
Advanced leadership, communication, and interpersonal skills, with the ability to work in a matrix environment and manage cross-functional teams.
Expertise in interpreting clinical trial data and understanding relevant pre-clinical and clinical data.
Medical Doctor (MD) degree.
Fluent in English (both written and spoken).
Ability to work effectively in a fast-paced environment and meet deadlines.

About Company

At Sanofi, we provide equal opportunities to all individuals, embracing diversity and inclusivity across all levels of the organization.

Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels before applying.

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