Sr. Clinical Research Associate

Added
21 days ago
Type
Full time
Salary
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Related skills

gcp training regulatory filings sops cross-functional liaison

πŸ“‹ Description

  • Manage full clinical site monitoring for one or more projects.
  • In-house based role; design and oversee monitoring services.
  • Train, recruit sites, manage data and regulatory filings.
  • Lead CRA as liaison between CRAs and project team.

🎯 Requirements

  • College diploma/degree with 4-6 years' experience.
  • Strong communication and self-motivation.
  • Attention to detail; build collaborative relationships.
  • Critical thinking abilities.
  • Ability to travel regularly.

🎁 Benefits

  • Home-based with regular travel.
  • Sign-on bonus for expansion phase.
  • Annual incentive program.
  • Mobile phone stipend.
  • Reimbursement for office equipment as needed.
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