support strategic decision-making. Duties: Invoicing Journals Budget, planning and forecasting Financial reporting guidance to management Education and Experience: BCom Studying CIMA is advantageous 2-3 years of experience minimum
support strategic decision-making. Duties: Invoicing Journals Budget, planning and forecasting Financial reporting guidance to management Education and Experience: BCom Studying CIMA is advantageous 2-3 years of experience minimum
Description Main purpose of the job: Support research studies for optimal implementation Location: 22 Esselen Johannesburg Key performance areas: Support the study team with any research-related activity Support prescribed reports for timely submission to the study coordinator/leadership team Assist in patient recruitment experience, and personal abilities: Research Internships and/or exposure to clinical trial working environment
Description Main purpose of the job: Support research studies for optimal implementation Location: 22 Esselen Johannesburg Key performance areas: Support the study team with any research-related activity Support prescribed reports for timely submission to the study coordinator/leadership team Assist in patient recruitment experience, and personal abilities: Research Internships and/or exposure to clinical trial working environment
finance department. Salary Cost Journals: Prepare monthly salary cost journals and review their accuracy for them against budget. Journal Entries Processing: Process payroll-related journal entries. Bank Reconciliations:
Description Main purpose of the job: The project manager/study coordinator is responsible for coordinating all activities according to good clinical practice, the study protocol, and the site's standard operating procedures protocol and GCP compliance Assist study team with efficient study start-up, conduct, and close-out Manage Manage regulatory updates throughout the study (New ICFs, Protocol Amendments, etc.) Proactively resolve investigators regarding participant welfare while on study Notify relevant parties of Serious Adverse Events
Description Main purpose of the job: The project manager/study coordinator is responsible for coordinating all activities according to good clinical practice, the study protocol, and the site's standard operating procedures protocol and GCP compliance Assist study team with efficient study start-up, conduct, and close-out Manage Manage regulatory updates throughout the study (New ICFs, Protocol Amendments, etc.) Proactively resolve investigators regarding participant welfare while on study Notify relevant parties of Serious Adverse Events
the job:
under-graduate studies - 2 days per module on 1st attempt) (Related post-graduate studies (CTA) - 20 days under-graduate studies - 2 days per module on 1st attempt) (Related post-graduate studies (CTA) - 20 days
performance areas: Inform participants about the study Screen potential participants and obtain informed informed consent according to SOPs Administer study questionnaires/interviews Draw blood/collect biological the fieldwork team if required Develop and update study-specific job aides Collect participant data from and other study documents Safekeeping of project assets Facilitate training of staff on study protocol timeously and accurately Provide regular updates on the study to key stakeholders Take ownership and accountability