Sr. Clinical Research Associate (Hungary)

Added
21 days ago
Type
Full time
Salary
Salary not provided

Related skills

gcp project management regulatory filings site monitoring sops
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๐Ÿ“‹ Description

  • Manage and deliver full clinical site monitoring for multiple projects.
  • Design and oversee monitoring services aligned with SOPs, GCP, and study guidelines.
  • Act as Lead CRA and primary liaison to project teams and CRAs.
  • Coordinate site recruitment, materials flow, and training.
  • Represent the company in sponsor communications and BD initiatives.

๐ŸŽฏ Requirements

  • College diploma/degree with 4-6 years of related experience.
  • Self-motivated with strong communication skills.
  • Strong attention to detail and collaboration.
  • Critical thinking abilities.
  • Ability to travel ~5โ€“8+ days per month.

๐ŸŽ Benefits

  • Home-based position.
  • Regular travel required.
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