Clinical Data Platform Expert

Il y a 5 heures

belgium be MSI Pharma Temps plein

IT Solution Expert - Clinical Data Acquisition Systems Location: Brussels Region, Belgium (Hybrid) Engagement: Freelance Client: Biopharma Competitive hourly rate available We are supporting a major biopharma organisation in hiring anIT Solution Expert to provide end‑to‑end support, maintenance, and enhancement of theirprimary clinical data acquisition platforms , including a suite of Medidata solutions and Trial Grid.You will act as the technical owner for system updates, validation activities, incident management, and change control while collaborating with internal teams and external platform providers. This is a high‑impact role supporting global clinical development operations.Key Responsibilities

  • Provide ongoingsupport and maintenance for the organisation’s Clinical Data Acquisition platform (incl. Medidata iMedidata, Rave, Coder, Cloud Admin and Coder+).
  • Support and maintain theTrialGrid system used to validate clinical study builds.
  • Assess the impact of new Medidata and TrialGrid product releases on availability, security, interfaces, and maintenance requirements.
  • DriveIT changes , including updates to computerized system validation documentation, IQ/OQ testing, and implementation of new/changed user requirements.
  • Performaccess management for designated user roles
  • Collaborate with SMEs to resolveincidents in alignment with ITIL best practice
  • Support theperiodic review of Clinical Data Acquisition and TrialGrid systems
Requirements Education
  • Bachelor’s degree (minimum) inComputer Science or a related field.
Experience & Technical Skills Mandatory:
  • Direct experience withMedidata platforms (e.g., iMedidata, Cloud Admin, Rave, Coder).
  • Proven experience incomputerized systems validation (CSV).
  • Experience incomputerized system testing .
  • Strong background inIT change management .
  • Experience handlingaccess management .
Preferred:
  • Experience withTrialGrid .
  • ITIL‑alignedincident management experience
  • Background in thepharmaceutical industry (3+ years preferred)
  • Knowledge ofClinical Development processes.
Soft Skills
  • Fluent inEnglish (written and spoken).
  • Strongtechnical documentation writing skills.
Excellentteam collaboration abilities.