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Ividata Life Sciences
Ividata Life Sciences
51 – 200 Employees
Food & BeverageHealthcareLogistics
Founded in 2013, Ividata Life Sciences is a French consulting firm supporting pharmaceutical, biotech, and other healthcare organizations throughout the product lifecycle. Its consultants work across three areas: biometrics and data, including biostatistics, data science, programming, bioinformatics, data management, and health economics and outcomes research; clinical operations, from epidemiology and real-world evidence to study management and monitoring; and regulatory affairs and pharmacovigilance, including submissions, safety monitoring, medical device registration, and advertising compliance. Ividata provides specialist consulting and staffing support for life sciences projects. The company reports a team of around 140 consultants across Europe.
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Medical Advisor Consultant

Support medical strategy, clinical studies, regulatory affairs, and scientific information. IVIDATA Life Sciences advises pharmaceutical, biotech, and healthcare organizations.

FRFranceHybridFull-timeMiddleSeniorEnglish RequiredFrench RequiredConsultant

Description

  • Help develop and track medical strategy across assigned therapeutic areas
  • Provide scientific expertise to clinical development, regulatory, pharmacovigilance, and medical communications teams
  • Build scientific relationships with healthcare professionals, researchers, and opinion leaders through expert committees and medical events
  • Keep scientific documentation aligned with ethical and regulatory requirements
  • Answer complex medical information enquiries
  • Review scientific literature on an ongoing basis
  • Train internal teams on medical advances and clinical data
  • Provide scientific and medical guidance throughout the product life cycle while maintaining rigor and regulatory compliance

Requirements

  • Doctor of Pharmacy (PharmD), PhD, or Master’s degree in Life Sciences
  • Initial or established experience in a medical position at a pharmaceutical company, biotech firm, or CRO
  • Strong knowledge of clinical trial methods and healthcare regulations
  • Strong interpersonal, analytical, and synthesis skills; clear communication; ability to support learning and collaborate across disciplines
  • Fluent in French and English

Benefits

  • A stimulating, collaborative work environment
  • Assignments with significant impact
  • Room to grow alongside dedicated experts
  • Work on major strategic projects advancing healthcare innovation
  • Contribute across the full product life cycle
  • Make a meaningful contribution through your ideas and expertise

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