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
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