Research interests

Worked on a number and variety of research studies in the care and management of research participants.

Used to coordinate the care of clients who were taking part in Phase I–IV trials, incl. ensuring all documentation and studies are carried out in accordance with ICH-GCP; supervision of research nurses; ensuring staff are trained to carry out roles and responsibilities.

As a CRC, managing clinical monitoring activities, incl. investigator/site selection, collating regulatory documentation, initiation and monitoring (source data verification, drug accountability and data collection) in accordance with ICH-GCP guidelines. 
 

Currently working as a Clinical Research Associates at the Dept. of Research Support on a number AMC Investigator Initiated trials .
 

Received ICH-GCP training/certification on: 28 May 2013, 05 Dec 2008, 6 Mar 2007, 27 Oct 2005 and 28 Jun 2001.
 

specialisation

Clinical Research Associate

ID: 3296390