San Francisco, CA
$185,000 - $210,000
Bachelor of Science
Mar 13, 2017
Outstanding opportunity for a Director of Quality for Clinical GCP. My client is seeking a talented Clinical Quality professional who has significant experience in ensuring that Clinical Trials are in compliance with Good Clinical Practice (GCP). Reporting in to the VP, this individual will be responsible for ensuring quality systems, procedures and documentation are in compliance with applicable US and international standards and regulations. While this is initially an individual contributor role, this is an opportunity to help to build a GCP function and later a team dedicated to clinical quality. This individual will have written standard operating procedures, systems and processes, have experience working with CRO's and clinical sites and be an experienced auditor. As this individual will provide training on GCP, excellent communication skills and an engaging personality are recommended. Strong attention to detail with auditing documentation and excellent team player with ability to interface with all levels of the organization. Should be comfortable functioning as a Lead Auditor.
The preferred candidate will have 10+ years of experience in the pharmaceutical or biotech industry with at least 5+ years of experience in the auditing of clinical trials. Excellent communication and collaborative skills and be a true team player.