Responsible for remotely supporting Iovance’s GCP quality system. • Support GCP quality system activities including clinical quality events, deviations, CAPAs, supplier corrective action requests, investigator site audits, service provider audits, internal audits, clinical change controls and regulatory inspections. • Identify opportunities to increase the efficiency and effectiveness of the GCP QMS. • Support training activities and back-up efforts for clinical quality assurance processes. • Maintain updated knowledge and relevant assessments of the GXP landscape, regulations, and guidelines pertaining to GCP quality assurance. • Some travel required (approximately 10%).
Iovance Biotherapeutics, Inc. is HIRING A
Clinical Quality Assurance Associate II
📍 United States 🌐 Fully Remote ⏰ Full TimePlease mention you found this job on TestDev Jobs. It helps us get more people to hire on our site. Thanks and good luck!