Job Summary
A company is looking for a Clinical Quality Assurance Associate to support the management of GCP-related items within the Quality Management System across clinical activities.
Key Responsibilities
- Ensure GCP compliance and promote best practices across regulated activities
- Investigate deviations and complaints, and follow up on CAPAs for timely resolution
- Review clinical trial documents and eTMF for accuracy and completeness
Required Qualifications
- Bachelor's Degree or higher in pharmaceutical, life sciences, or engineering concentration
- 0-3 years of experience in a Quality-related role with exposure to GCP activities
- Familiarity with eTMFs and proficiency in Microsoft Office
- Knowledge of ICH GCP guidelines and relevant regulatory requirements
- Self-motivated and proactive with strong organizational skills
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