Company Aurum Group
Reference # Opt4TPTREF003
Contract Type Permanent
Salary Market Related
Location Johannesburg, Gauteng, South Africa
The Aurum Institute is offering a great opportunity to suitably qualified and experienced staff to contribute towards our mission to improve the health of people and communities through innovation in Health Research and Systems. We are focused on research, support and implementing integrated approaches to managing TB and HIV. The following positions have become available as part of the various projects currently being run by us and you are welcome to apply should you meet the requirements of the position.
Job Functions Medical
Industries Medical,Ngo / Non-Profit
Your primary role will be to participate in:
Participant recruitment and enrolment
Recruit potential participants for the study
Ensure that potential participants are provided with all the study details as described in the Participant Information Sheet.
Administer written informed consent
Recruit and schedule appointments for qualitative study participants
Assist study coordinator to plan recruitment schedules
Conducting enrolment activities
Research related activities
Being responsible for the proper documentation of all study activities
Administer data collection instruments as required.
Collect adherence data from electronic data monitoring devices
Transcribe qualitative interviews sessions
Perform quality checks on collected data.
Data query resolution
Complete any other activities as required by the protocol or the study.
Complete, compile and submit study case report forms (CRFs) and source documents timeously
Ensure all records on participants are completed and accurately filed with strict adherence to documentation handling procedures
Maintain accurate study logs related to enrolment and other study activities.
Report on daily/weekly activities to the Study Coordinator and meet stipulated enrolment and follow-up targets
You will also be required to retain participants by;
Obtaining, verifying and updating detailed locator data from participant for all visits.
If possible, reminding participants about their appointments just prior to each visit
Following-up on participants to ensure study completion
Recommending retention strategies to study management
You will be required to;
Prepare participant files and documents.
Reconcile reimbursement of participants
Safe storage and transportation of complete study documents
Attend study meetings to report on study progress