- Help the investigator in screening patients
- Assisting investigators in the Informed Consent Process
- Coordination and management of laboratory samples, courier and follow-ups of lab reports
- Drug accountability and dispensing at the site
- Investigational product management, dispensing, temperature monitoring and accountability
- Preparation, attendance and follow-up of monitoring
- Completing CRF entry
- Preparation, attendance and follow-up of Audit
- Preparation & forwarding the necessary information of closeout
- Prepare the required documents for submission to the Ethics Committee
- Initiating and submitting for Ethics Committee approval
