Sr. Clinical Research Associate (Netherlands)

Added
18 days ago
Type
Full time
Salary
Salary not provided

Related skills

gcp sops

๐Ÿ“‹ Description

  • Manage full clinical site monitoring for multiple projects.
  • Design/oversee monitoring including training, recruitment, data/doc mgmt.
  • Oversee site budgets and regulatory filings per SOPs and GCP.
  • Lead CRA role; liaison between CRAs and project team.
  • Contribute to project plans, protocols, CRFs, communications.
  • Represent company and maintain stakeholder relationships.

๐ŸŽฏ Requirements

  • Bachelor's degree or higher; 4โ€“6 years related experience.
  • Strong communication and self-motivation.
  • Attention to detail; collaborative relationships.
  • Critical thinking abilities.
  • Travel 5โ€“8+ days per month.
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