Clinical Research Associate
vor 2 Wochen
Job Summary:
As a Clinical Research Associate, you will play a crucial role in ensuring the success of our clinical trials. Your primary responsibility will be to conduct site monitoring visits to ensure compliance with ICH GCP guidelines and company SOPs. You will also be responsible for preparing accurate and timely monitoring visit reports, as well as conducting source document review and verification.
Key Responsibilities:
• Perform qualification, initiation, and close-out visits at clinical trial sites
• Prepare accurate and timely monitoring visit reports
• Conduct source document review and verification
• Ensure compliance with ICH GCP guidelines and company SOPs
Requirements:
• BS/BA in a relevant field
• 2 years of clinical research experience
• Strong organizational skills
• Problem-solving abilities
• Excellent communication and interpersonal skills
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