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Provide overall management of clinical trials or clinical programs within Wits DIHKey performance areas:Drafting of Quote as per protocol requirementsConvert research protocol into workable analytical/study plans to enable the laboratory staff to conduct necessary testsAssist with services agreements if required for sponsorEnsure project and protocol amendments are implemented as required
All study projects are set up according to Good Clinical Laboratory Practice , Good Clinical Practice Take primary responsibility for the response to project audit findings related to CT department specific to the project Prepare project status and other administrative reports and submit to sponsors and other internal stakeholders as required by the contract
Report timeously on project progress, the results of risk analyses, contingency plans, technical information, and input from team throughout the projectProcess validation: All dry run documents must be completed and reviewed by all CLS departmentsCommunicate any significant changes in resourcing, scope of work and timelines to all stakeholders including team membersNational Diploma in Medical Technology or BSC in Health Sciences or relevant work experienceDesirable additional education, work...
Completion of Good Clinical Laboratory Practice and Good Clinical Practice courses will be advantageousProject management experience will be advantageousAbility to operate in a pressurized environmentGood Interpersonal and communication skills with both internal and external stakeholdersOnly if you do meet the minimum job requirements and experience as mentioned above, you may submit a detailed updated CV.
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