Document Coordinator Data Collection (Mid) – Data Sc
GMP Document Coordinator
Hybrid Role – 3 days onsite. Monday – Friday 7am-4pm scheduled preferred.
Assist Clinical Supply Manager with developing records and executing records to prepare study medication.
Responsibilities:
Scanning and Filing documents into an electronic system
? Appropriate naming each document
? Filing the document into the system
? Prepare shipments, issue FedEx Labels and track shipments
? Handle returned study medication and prepared for storage
? Monitor expiration dates
? Maintain inventory of secondary packaging material
Qualifications:
? Must have previous experience in cGMP environment
? Experience with cGDP is a plus
Last Date For Apply: 2024-06-20 00:00:00 Job Type : FULL_TIME, Employment Type : FULL_TIMEApply Here