Reception duties including making appointments for patients at the surgery Doing hospital bookings and booking the theatre at the hospital as required Involved with research as a Study Coordinator with Dr. Oosthuysen under Limaro Research Managed multiple clinical trials simultaneously. Responsible for all day-to-day activities necessary to facilitate the successful completion of each study.Trained clinic personnel to effectively complete study specific procedures and documentationPrepare and completion of all feasibility documentation, documents for Ethics and MCC submission. Reading of Informed Consent Form to ensure accuracy according to ICH GCP. Ensure that ICF is done according to SOP and ICH GC. Evaluated and analyzed clinical research data to ensure accuracy and consistency between source documents and study documents as well as proper, timely reporting of critical study eventCompiling of source documentation, formatting and editing of the existing documentation.Prepared and assisted in preparation for Sponsor and IRB audits.Responsible for identifying new protocols and implementing them. Storing/Archiving of study documents according to site SOP. Used different Electronic Data System to enter data. Quality assurance and control of transcription of all data from source documentation to electronic case report forms. Establishing Standard Operating Procedures and streamlining processes to ensure proper support of clinical faculty. Reviews and accepts/corrects the billing matrix as set up by the Sponsor to facilitate billing of study procedures to the appropriate research fund. Coordinate appropriate and timely payments to participants in accordance with SOP and procedures.Acquire calibration documents for site equipment.

Patient liaison Drawing blood from patientsMaintains documentation of training. Dealing with clients