Research Technologist: Data Coordinator
at South African Medical Research Council MRC
Durban, KwaZulu-Natal, South Africa -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 30 Sep, 2024 | Not Specified | 26 Sep, 2024 | 1 year(s) or above | Clinical Trials,Clinical Research Experience | No | No |
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Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
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Contract to Hire – Corp 2 Corp |
Description:
CORE REQUIREMENTS:
- 1- or 2-year accredited course/certificate relevant to the job/discipline or similar relevant qualification or higher
- At least 2 years clinical research experience
- At least 1-2 years’ experience in conducting data activities in clinical trials.
- At least 1-2 years’ experience in electronic data capturing and QC resolution.
Responsibilities:
RESPONSIBILITIES:
- Ensure optimum data quality in clinical trial research documentation (source, CRFs and Electronic Data Capture System)
- Quality Control of all study documentation including informed consent process. Maintain QC rate within acceptable levels across multiple studies.
- Perform regular data checks on the database and generate data reports. Corrective action of reports from the database and corrective action/responding to emails received from the study data manager.
- Ensure that staff QCs are completed timeously. Provide ongoing support to staff completing data capture and addressing QCs. Assisting with troubleshooting for system issues.
- Electronic data capture within the protocol-specified time frames for multiple studies
- Assist with preparation for monitoring visits and corrective actions for internal and external monitoring reports for multiple studies.
- Documentation management including version control of all study related documents.
- Maintaining an excellent filing and indexing system for all study documents including participant and regulatory documents
- Assist with setup and implementation of new studies.
- End of study document inventory
- Development and preparation of reports for study management
PLEASE QUOTE THE REFERENCE NUMBER (R779A) IN ALL COMMUNICATIONS. PLEASE BE ADVISED THAT YOUR SUBMISSION WILL NOT BE CONSIDERED SHOULD YOUR APPLICATION NOT BE ACCOMPANIED BY THE REQUIRED INFORMATION AND DOCUMENTATION.
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REQUIREMENT SUMMARY
Min:1.0Max:2.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Trade Certificate
1- or 2-year accredited course/certificate relevant to the job/discipline or similar relevant qualification or higher
Proficient
1
Durban, KwaZulu-Natal, South Africa