Quality Control Officer at CAPRISA

CAPRISA has an opportunity for a suitably qualified and experienced candidate with previous experience in clinical research to fill the role of Quality Control Officer based at the Vulindlela Clinical Research Site (Howick area).

Minimum Requirements    

• At least 2 years of research experience, preferably in a data management/regulatory affairs role, with an understanding of HIV/AIDS research.
• Grade 12, with a tertiary qualification in Health/Social Sciences is an advantage
• High level of computer literacy essential, with demonstrated experience with iDatafax, iMedidata Rave, REDCap and/or other Clinical Trial software

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

Duties & 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