Clinical Research Associate - BioPharmaceutical

Typical Accountabilities:
• Ensures the processes for Study Delivery are executed through the development of study reports tools, facilitation of the study delivery system and maintenance of the system.

• As an expert, ensures delivery of a centrally managed study management service across clinical studies from start up to reporting

• Serve as main contact and works closely with the Document Management group until the Clinical Study Report is finalised

• Initiates and maintains production of study documents, ensuring template and version compliance

• Creates or imports clinical-regulatory documents into the Global Electronic Library according to the Global Document List

• Interfaces with Data Management Centre or Data Management Enablement representatives to facilitate the delivery of study related documents

• Manages and coordinates tracking of study materials and equipment

• Monitors administrative tasks during the...