Grade 12 or equivalent certificate.
Computer literacy is essential (MS Office).
Strong numerical skills.
A professional, mature and calm person with independent problem solving abilities within a busy environment.
Experience in a similar environment.
A client orientated person with the ability to treat information confidentially.
Co-ordinate, implement and manage clinical trials in one or more therapeutic areas, including investigator selection, study initiation, monitoring, closure and archiving of study documentation.
Manage a team of up to 6-7 CRAs/CRO staff according to size portfolio and/or therapeutic area.
Key Purpose The Coordinator would play a key role in an integrated funder-provider programme designed to co-ordinate the care of a carefully selected group of DH members by actively identifying patients that meet our clinical entry criteria.
Key Purpose To comprehensively investigate and respond to complaints lodged at the Council for Medical Schemes and provide feedback to business on the root causes of the complaints.
Key Outputs Successful applicant will be responsible for, but not limited to the following job functions: