company in Germiston seeks a Technical chemical analyst. Going around to customers Picking up samples Inspecting
VETERINARY SCIENCE DEPARTMENT OF COMPANION ANIMAL CLINICAL STUDIES PROFESSOR / ASSOCIATE PROFESSOR / SENIOR Planning and managing the academic, research and clinical programmes of the Department, including the training leadership in transformation initiatives; The clinical services rendered by the clinicians and specialist Hospital, surrounding community and satellite clinics, including a 24-hour service in conjunction with co-author; Experience with student supervision (clinical and academic); At least 5 years significant experience
will be responsible for participant recruitment and data collection at the allocated study sites
will be responsible for participant recruitment and data collection at the allocated study sites
will be responsible for participant recruitment and data collection at the allocated study sites
will be responsible for participant recruitment and data collection at the allocated study sites Where appropriate participants, in line with study protocol, SOPs and Good Clinical Practice Conduct Informed Consent discussion according schedule Conduct data extraction from clinic registers, patient records or other relevant data sources as per manage and maintain quality data for research and operations purposes. Capture data into study databases e Identify missing data, inconsistencies, and errors and follow up or report on missing data or errors Support
will be responsible for participant recruitment and data collection at the allocated study sites Where appropriate participants, in line with study protocol, SOPs and Good Clinical Practice Conduct Informed Consent discussion according schedule Conduct data extraction from clinic registers, patient records or other relevant data sources as per manage and maintain quality data for research and operations purposes. Capture data into study databases e Identify missing data, inconsistencies, and errors and follow up or report on missing data or errors Support
will be responsible for participant recruitment and data collection at the allocated study sites Where appropriate participants, in line with study protocol, SOPs and Good Clinical Practice Conduct Informed Consent discussion according schedule Conduct data extraction from clinic registers, patient records or other relevant data sources as per manage and maintain quality data for research and operations purposes. Capture data into study databases e Identify missing data, inconsistencies, and errors and follow up or report on missing data or errors Support
will be responsible for participant recruitment and data collection at the allocated study sites Where appropriate participants, in line with study protocol, SOPs and Good Clinical Practice Conduct Informed Consent discussion according schedule Conduct data extraction from clinic registers, patient records or other relevant data sources as per manage and maintain quality data for research and operations purposes. Capture data into study databases e Identify missing data, inconsistencies, and errors and follow up or report on missing data or errors Support
will be responsible for participant recruitment and data collection at the allocated study sites Where appropriate participants, in line with study protocol, SOPs and Good Clinical Practice Conduct Informed Consent discussion according schedule Conduct data extraction from clinic registers, patient records or other relevant data sources as per manage and maintain quality data for research and operations purposes. Capture data into study databases e Identify missing data, inconsistencies, and errors and follow up or report on missing data or errors Support