Job Summary
A company is looking for a Clinical Quality Compliance Lead to provide guidance on inspection readiness and compliance in clinical trials.
Key Responsibilities
- Provide just-in-time guidance to study teams on operating model processes and documentation for inspection readiness
- Manage inspection readiness planning and oversee TMF performance and compliance processes
- Facilitate study team preparedness for audits and inspections, ensuring effective communication and issue escalation
Required Qualifications
- Minimum of 6+ years of clinical research experience in the pharmaceutical or biotechnology field
- Solid knowledge of GCP compliance and regulatory inspection readiness
- Experience with CROs and outsourced clinical trial activities
- Bachelor's degree preferred or equivalent experience
- Proven project management skills and ability to work in a fast-paced environment
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