Clinical Research Associate
1 month ago
Job Summary:
SGA Fortrea Pharmaceutical Research & Development (Beijing) Co Ltd, Guangzhou Branch is seeking a highly motivated and detail-oriented Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for conducting site monitoring visits, ensuring compliance with regulatory requirements, and providing support to clinical trial teams.
Key Responsibilities:
• Conduct site monitoring visits to ensure compliance with regulatory requirements and study protocols
• Verify informed consent procedures and protocol requirements are adhered to
• Review source documents to ensure data integrity and accuracy
• Identify and report any deviations or issues related to the study
• Collaborate with clinical trial teams to ensure timely and efficient completion of studies
Requirements:
• 6 months experience in a related role (e.g. site management, in-house CRA, study coordinator, research nurse, etc.)
• Basic understanding of Regulatory Guidelines
• Ability to work within a project team
• Good planning, organization and problem solving skills
• Good computer skills with good working knowledge of a range of computer packages
• Works efficiently and effectively in a matrix environment
• Valid Driver's License
Education/Qualifications/Certifications and Licenses:
• University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure). An equivalent amount of experience can be substituted as appropriate.
• Basic knowledge of Regulatory Guidelines
• Basic understanding of the clinical trial process
• Fluent in local office language and in English, both written and verbal
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