Sr. Clinical Research Associate (Romania)

Added
20 days ago
Type
Full time
Salary
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Related skills

gcp project management clinical research site monitoring regulatory
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๐Ÿ“‹ Description

  • Manage full clinical site monitoring for one or more multinational projects.
  • Design and oversee monitoring services: training, site recruitment, data.
  • Lead CRA on large/complex projects; develop plans, CRFs, communications.
  • Act as primary liaison between CRAs and project teams; escalate issues.
  • Represent company in BD initiatives with monitoring focus.

๐ŸŽฏ Requirements

  • College diploma/degree plus 4-6 years of related experience.
  • Strong communication, self-motivation and results orientation.
  • Attention to detail and ability to build collaborative relationships.
  • Commitment to continuous learning and self-development.
  • Ability to foster teamwork across cross-functional groups.

๐ŸŽ Benefits

  • Home-based role
  • Regular travel required
  • Multinational project exposure
  • Training and professional development
  • Collaborative cross-functional teams
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