Sr CRA I (sponsor dedicated) Denmark

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Full Remote
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Offer summary

Qualifications:

Bachelor's degree in life sciences or related field., Minimum of 3 years of experience in clinical research., Strong knowledge of GCP and regulatory requirements., Excellent communication and organizational skills..

Key responsibilities:

  • Manage and monitor clinical trial sites to ensure compliance.
  • Conduct site visits and maintain relationships with investigators.
  • Prepare and review study documentation and reports.
  • Collaborate with cross-functional teams to support trial execution.

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Syneos Health Large http://www.syneoshealth.com
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