• Create (from-scratch) and/or significantly rewrite documents including but not limited to design history files, design verification records, and master production records. • Master technical information, organize content, and imbed GxP compliance •...

SUMMARY: This position assists in developing and implementing short term and long-term clinical supply chain strategies and networks to manage clinical supplies and their distribution whilst effectively managing challenges encountered within supply...

SUMMARY: Responsible for the design, documentation, implementation and execution of data collection and data quality review in clinical research studies. ESSENTIAL DUTIES AND RESPONSIBILITIES: • Provide expertise in data management to support...