: Associate Director, Clinical Program Quality Investigations is responsible for ensuring the compliance of deviation management... and Serious Breach process across Clinical Program Quality. Acts as Subject Matter Expert (SME) for clinical deviation management...
and modest costs. SUMMARY: Associate Director, Clinical Quality Assurance The Associate Director, Clinical Quality... industry standards and practices. The Associate Director, CQA will lead and perform day-to-day clinical quality operations...
Associate Director, Clinical and Safety Quality Compliance is responsible for ensuring the quality of processes and product... with functional compliance teams for regulations impacting Clinical, Safety and Clinical Pharmacovigilance Medical Quality (CPMQ...
Job Description General Summary: The Associate Director of QC Raw Materials manages and directs the Vertex cell... and guidance for the resolution of investigations, deviations, CAPAs, change controls, and other quality systems issues...
Job Description The Associate Quality Director conducts quality assurance oversight and management activities... manufacturing facilities. Serves as the Quality Lead for assigned clinical programs providing GCP compliance interpretation...
Job Description The Associate Director, Quality Assurance CMO Management is responsible for supporting the day-to-day... in relevant geographies at periodic intervals on site at the CDMOs. Participate in Cell & Genetic Program and Quality projects...
Job Description General Summary: The Biostatistics Associate Director will perform sophisticated scientific... with statistical programming and other functions to ensure timely delivery of TFLs with high quality. Contributes to clinical study...
and implementation of a clinical or pharmacovigilance audit program, hosting/leading regulatory inspections, investigations... to enable optimization of clinical and safety quality compliance activities. Provide expert advice and support to the CPMQ team...