Job Summary
A company is looking for a Clinical Quality Compliance Lead.
Key Responsibilities
- Evaluate clinical trial processes for adherence to documentation and engage with study team representatives
- Develop and maintain KPIs, metrics, and dashboards for tracking process quality and compliance
- Provide feedback on study process, documentation quality, and team performance
Required Qualifications
- Minimum of 4+ years clinical research experience in pharmaceutical or biotechnology field
- Solid knowledge of drug development, clinical trial management, and GCP compliance processes
- Proven track record in managing projects related to clinical trial delivery or compliance activities
- BS, MS or equivalent in a scientific field
- Experience with Microsoft Office and project management software
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