About the Job
We arean innovative global healthcare company with one purpose: to chase the miracles of science to improve people's lives.We'realso a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people,and stretch the limits of what you thought was possible. Ready to get started?

The main purpose of the CDS job role is to collaborate with the physicians, assisting GPH, Clinical lead and CRDs in activities around the compound, MA interactions, support in literature reviews, and follow some development activities as post-commitment studies.

The new recruiter will work with a team composed of clinical development experts, statisticians, clinical operations personnel, medical writers, safety experts, regulatory affairs, medical affairs and external key opinion leaders. He/She will develop some medical competencies in the disease and experimental therapy for which he/she is responsible.

• Work with development physicians for the preparation of supportive documents for AdBoards and meetings with Regulatory Affairs
• Literature review update related to external opportunities
• Participates to the review of the list of countries for clinical studies and ensures alignment with Medical Affairs and Commercial teams on the business case for each country
• Compiles regulatory, launch and reimbursement status in collaboration with regulatory, commercial and market access teams.
• Collaboration and interaction with the Project Team members and the Project Leader and with the other departments of the Neurology TA (clinical pharmacology, Global Safety Officer, biostatistics, regulatory, Medical affairs and commercial teams) to facilitate the preparation of deliverables that need various contribution.
• Contribute to the preparation of clinical sections of protocols, key result memo, clinical study reports, regulatory agency update reports, and other clinical and regulatory documents with focus on more routine/standard document elements describing all clinical procedures/ or studies to be included in this respective documents.
• Participates to the review of scientific publications and communications to ensure data accuracy with source documentation such as CSR.
• Provides support for the preparation of presentations used for different committees (BRAC, TARC, , , GPTM, STF, DWG...)
• Participate at Global program level meetings, such as, , GPTM, , STF Requested Profile
• Educational background: Scientific medical degree (PhD) with strong experience (>10 years) in Pharma business across different entities (R&D and Medical Affairs)
• Experience in KOL interactions, in data review and interpretation, in manuscripts and abstracts preparation
• Knowledge of Pharmacovigilance and CMC landscape, of project planning tools
• Understanding of clinical research process from program planning to regulatory submission

• Bring the miracles of science to life alongside a supportive, future-focused team.
  
• Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally.
  
• Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
  
• Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks' gender-neutral parental leave.