Clinical Research Associate I/ Clinical Research Associate II

Added
2 days ago
Location
Type
Full time
Salary
Salary not provided

Related skills

clinical trials site monitoring regulatory submissions oncology sops

📋 Description

  • Monitor and own progress of clinical studies at investigative sites.
  • Ensure studies conducted, recorded and reported per protocol and ICH-GCP.
  • Coordinate site setup and monitoring (investigators, submissions, visits).
  • Remote-based role with travel to sites; Paris area preferred.
  • Focus on oncology and rare diseases; collaborative culture.

🎯 Requirements

  • Life science degree or equivalent experience.
  • 1+ year CRA experience in CRO or pharma.
  • Experience managing oncology studies.
  • Domestic travel incl. overnight stays; international travel may be required.
  • Excellent communication and organizational skills.
  • English plus local language proficiency where applicable.
  • Study startup activities experience (preferred).

🎁 Benefits

  • Remote-based position with travel to sites.
  • Travel up to 50-60%.
  • Influence and impact with direct line management support.
  • Join a team focused on oncology and rare diseases.
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