Sr. Clinical Research Associate (Serbia)

Added
20 days ago
Type
Full time
Salary
Salary not provided

Related skills

travel gcp regulatory filings sops crfs
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๐Ÿ“‹ Description

  • Manage, deliver and/or perform full clinical site monitoring for one or more projects.
  • In-house role designing and overseeing project monitoring.
  • Includes training, site/patient recruitment, and data management.
  • Oversee budgets and regulatory filings; ensure SOPs and GCP.
  • Lead CRA liaison between CRAs and project team; assist in plans & CRFs.
  • Represent the company in meetings and maintain stakeholder relations.

๐ŸŽฏ Requirements

  • Minimum college diploma/degree with 4-6 years of related experience.
  • Self-motivation with strong communication skills.
  • Attention to detail and collaborative mindset.
  • Critical thinking abilities.
  • Ability to travel regularly to sites (Bosnia and Croatia).

๐ŸŽ Benefits

  • Home-based, with regular travel.
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