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Director of Quality Assurance and Compliance
hace 2 meses
Biorasi is seeking a highly experienced and skilled Associate Director of Quality Assurance to join our team. As a key member of our Clinical Operations department, you will be responsible for leading the development, implementation, and maintenance of our Quality Systems and Standard Operating Procedures (SOPs).
Key Responsibilities- Lead the development, implementation, and maintenance of GCP Quality Systems and SOPs.
- Train and mentor staff on global GCP regulations and guidance.
- Provide QA oversight and auditing of eTMFs.
- Lead and/or oversee consultant-mediated audits; develop, recommend, and follow up on corrective actions.
- Lead preparations for Clinical Operations (corporate and third-party) inspection-readiness.
- Lead and manage GCP Inspections on behalf of Biorasi and Biorasi clients.
- Serve as an SME for areas of responsibility during regulatory inspections, and directly manage inspection Ready-Room activities.
- In partnership with the Clinical Operations, Regulatory, and Pharmacovigilance teams, design and implement a risk-based clinical Quality Assurance management system.
- Identify QA and compliance-related issues and implement solutions to ensure timelines are maintained.
- Establish metrics and report the state of GCP Quality and compliance of clinical trials to senior management.
- Ensure Clinical Operations activities are compliant with cGCP, cGLP, FDA, ICH, EMA regulations and guidelines and industry standards.
- Provide consultation in interpretation of regulations/guidelines, as they apply to GCP practice, awareness of regional regulatory requirements, and phase of study.
- Keep abreast of industry developments – forthcoming regulations, guidance, best practices, etc.
- Ensure that Biorasi quality systems, processes, and procedures are compliant with applicable regulations and ICH guidelines.
- Ensure that Biorasi standard operating procedures (SOPs) are compliant with applicable regulations and guidelines.
- Oversee the planning and conduct of internal, investigator, and vendor Quality Assurance audits.
- Manage the administration of Quality Assurance files and the control of central files.
- Degree in biomedical sciences or related scientific discipline.
- 10+ years in drug development or clinical research within the pharmaceutical industry or CRO with at least three years in quality assurance, quality management, or clinical safety-related area of responsibility.
- Strong planning, leadership, negotiation, communication, and presentation skills.
- Experienced with auditing clinical vendors and investigator sites.
- Practical knowledge of GCP or GMP, and FDA regulatory structure.
- Proficient with Microsoft Office tools.
