Clinical Research Coordinator (Clinical Research Operations Support)

Primary Responsibilities

As a member of the team in our Global Business Solutions (GBS) center, responsible for managing and reviewing and filing study documents that are used on clinical trials. This position is also responsible for written and verbal correspondence with the internal team as well as regulatory authorities, ethics committees, investigators, monitors, and sponsors.

Specific Responsibilities

• At all times, complies with SGS Code of Integrity and Professional Conduct.
• Responsible for maintaining the filing system and managing the central study documentation (TMF/ISF)
• Assists in the development of study documents and study submission.
• Assists with written and verbal correspondence with regulatory authorities, ethics committees, investigators, monitors, and sponsors Assists in the reviewof study documents.
• Assist with the development and updating of SOPs, Work...