Responsibilities

  • Provide RIM expertise and consulting to clients
  • Lead and support RIM implementation projects
  • Advise clients on IDMP compliance and xEVMPD
  • Manage regulatory data and systems
  • Act as a project leader and coordinate stakeholders
  • Contribute to IT and regulatory system integration

Requirements

Profile Required

  • Background in Life Sciences or IT
  • 5–10 years of experience in Regulatory Affairs / RIM
  • Experience in the pharmaceutical industry is a strong plus

Technical Skills

  • Strong expertise in Veeva Vault RIM / Ennov RIM
  • Knowledge of IDMP & xEVMPD standards
  • Advanced Excel skills (Power Query)

Languages

  • English required
  • French is a plus

Soft Skills

  • Autonomous and organized
  • Strong analytical and problem-solving skills
  • Ability to lead projects and manage priorities
  • Adaptable with a client-oriented mindset

Publish Date

03 August, 2026

Spontaneous Application

RIM Expert - VAF 540

New opportunities open up across PLG all the time. If nothing matches right now, send us a spontaneous application: we will keep you in mind for what comes next.

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