Quality Control Officer - Durban at CAPRISA

Minimum Requirements

• Tertiary qualification in Health Sciences an advantage
• At least 2 years of research experience, preferably in a date management/information role, with an understanding of HIV/AIDS and TB research
• High level of computer literacy essential, with demonstrated experience with Clinical Trial software
• Microsoft Office experience
• Personal Qualities and Competencies
•  Attention to detail, with strong analytical ability
• Ability to organize and manage multiple priorities
•  Ability to work independently, without direct supervision and fit in well within a multi-disciplinary team
•  Excellent communication and interpersonal skills

Key Responsibilities

•  Responsible for the review and verification of all source data to ensure the completeness, accuracy and consistency of source data
•  Recommend and monitor corrective and preventive actions
• Ensure data corrections are completed according to GCP guidelines and reviews are completed based on study protocols / SOP’s and within study specific timelines
•  Prepare reports to communicate the outcome of all quality activities
•  Identify training needs and schedule training interventions to address the requirements for all quality standards