Senior Associate, Central Monitor, Data Surveillance, Clinical Data Sciences

About the role

The Senior Associate, Central Monitor is responsible for ensuring the completeness, quality and integrity of the subject data in the clinical trial database under Risk Based Monitoring (RBM) mode.

What you'll do

• Responsible for ensuring the completeness, quality and integrity of the subject data in the clinical trial database under Risk Based Monitoring (RBM) mode
• Implement quality oversight/control steps implemented in the central monitor activities
• Review protocols to ensure the set-up, review and reporting requirements can be met and are standardized
• Provide technical oversight, guidance and coordination for all the central monitor activities

What you need

• Any graduate