Clinical Scientist

Sanofi

Gentilly, France
Onsite
Clinical study execution
Medical scientific documents
Clinical trial set-up
The primary purpose of the Clinical Scientist’s position is to assist/support the Clinical Research Director (CRD) in the medical/scientific contribution for the clinical studies, on activities pertaining to the Study Medical Manager responsibilities

Job Summary

  • The primary purpose of the Clinical Scientist’s position is to assist/support the Clinical Research Director (CRD) in the medical/scientific contribution for the clinical studies, on activities pertaining to the Study Medical Manager responsibilities.
  • He/she ensures appropriate review and consistency of the data and investigations of safety cases with the Clinical Trial Team (Monitoring Teams) or Pharmacovigilance.
  • Maintain scientific, technical, and clinical expertise in immunology, dermatology, pulmonology, or other disease areas within the Immunology and Inflammation therapeutic area.

Matching Summary

The primary purpose of the Clinical Scientist’s position is to assist/support the Clinical Research Director (CRD) in the medical/scientific contribution for the clinical studies, on activities pertaining to the Study Medical Manager responsibilities.

Skills & Requirements

Must-have

  • clinical study execution
  • medical scientific documents
  • clinical trial set-up
  • data validation and review
  • cross-functional global teams

Nice-to-have

  • open transparent collaborative working style
  • good leadership interpersonal skills
  • driven individual performance oriented
  • problem solving conflict resolution

Key Requirements

  • Advanced degree preferred (PharmD or PhD scientist or Biomedical Science master with previous experience in Clinical Research and/or Clinical Drug Development)
  • 2+ years of industry experience (clinical development)
  • Strong English skills (verbal and written)
  • Experience with supporting preparation and execution of clinical trials
  • Experience with interaction with regulatory Authorities for clinical trials is a plus
  • Experience with basic statistical principles and techniques of data analysis
  • Proven ability to manage projects/team of significant scope and complexity

Work Rights

Not specified

Tailored Resume

Cover Letter