Das ist der Job
Support the Quality Management System including SOPs, training, and CAPA processes.
Darum lohnt es sich
Availability to travel up to 25% domestically and/or internationally. Host client/sponsor audits and support regulatory inspections. Coordinate and conduct vendor, internal, investigator site, and trial master file audits. Qualifications: Extensive working knowledge of GCP Process Audits. Bachelor's degree in science, healthcare, or related field.
Preferred Experience: CRO experience and QA certification (e.g., CQA, SQA) preferred. Experience with electronic clinical trial systems (e.g., EDC, CTMS, IxRS, ePRO). #J-18808-Ljbffr
