Job Description
Works with assigned clinical research project teams
Responsible for the background administration and preparation for trial set up, monitoring, tracking and close out
Assisting in the organisation of investigator, project team and client meetings
May assist in preparation of Regulatory and Ethics Committee packages
Maintain study status tracking forms, trial supplies dispatch and receipt records, investigator payment records, etc
Maintain tracking databases
Other ad hoc tasks associated with clinical trials and office administration as required
Requirements
nursing or life science background
good at oral & writen english
Interest in Clinical Research
Pls send a CV to
[email protected], if interested.