Associate Director of Process Development and Documentation | Clinical Quality Assurance (CQA)
ONSITE SAN FRAN 3x PER WEEK - RELO PACKAGE OFFERED
Professional Summary: A highly experienced Clinical Quality Assurance professional with over 10 years of expertise in developing and maintaining clinical research SOPs, process development, and compliance for clinical-stage pharmaceutical companies. Proven leader with strong technical writing skills, capable of working cross-functionally to ensure adherence to industry standards and regulatory requirements. Experienced in managing audits, inspections, and continuous improvement of the Quality Management System (CQMS).
Key Skills & Expertise:
Professional Experience:
Education:
Bachelor of Science (BS) in Biological Sciences (or related field)
Technical Skills:
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