needs, and monitoring Good Clinical Laboratory Practice compliance. Assist clinical site laboratories
needs, and monitoring Good Clinical Laboratory Practice compliance. Assist clinical site laboratories
study site documentation following Good Clinical Practice Assist with any outstanding ethics application
study site documentation following Good Clinical Practice Assist with any outstanding ethics application
site documentation following Good Clinical Practice
Conduct Quality Control activities for clinical trials, assist with regulatory communications and adherence
onduct Quality Control activities for clinical trials, assist with regulatory communications and adherence
Conduct Quality Control activities for clinical trials, assist with regulatory communications and adherence
Qualifications:
Tertiary degree required in the Natural Sciences or Engineering
Minimum of 2 Years working experience
Competencies: