advantageous Previous knowledge and experience with international quality standards will be advantageous Must responsibilities are done on a daily basis (international quality standards) • Maintain control of retention samples in the QC lab • Assist with investigating of internal and external NCRs • Assist with writing and revising
Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor, and regulatory authorities requirements Compliance with all relevant SOPs Communicate well with investigators regarding participant
Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor, and regulatory authorities requirements Compliance with all relevant SOPs Communicate well with investigators regarding participant