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Medical Technologist (Clinical Pathology - WITS RH

5 months ago1426 views
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General Details
Advertised By:Agency
Company Name:Executive Placements
Job Type:Full-Time
Description
Main purpose of the job:
  • To perform on-site laboratory processes and ensure efficient workflow of the onsite laboratory
Location:
  • 7 Esselen Street, Hillbrow, Wits RHI Research Centre Clinical Research Site (CRS)
Key performance areas:
  • Co-ordinate all daily lab activities to ensure work is completed within turnaround time
  • Ship samples to outsourced laboratories
  • Follow up on DCF and final reports within TAT
  • Communicate laboratory results to doctors/nurses/site coordinators effectively and timeously
  • Provide technical input on laboratory results (within scope of practice)
  • Perform laboratory equipment maintenance
  • Lab decontamination and temperature surveillance in the onsite laboratory
  • Perform backup duties at other Wits RHI on-site labs when requested to do so
  • Perform troubleshooting activities as and when required and ensure communication to the Lab Manager
  • Perform duties per study Delegation of Authority Logs
  • Ensure equipment maintenance is performed as per maintenance schedules and SOPs
  • Monitor and control stock levels and ensure sufficient stock is available such that lab activities are not adversely affected
  • Timeous and logical filing of all laboratory records
  • Demonstrate cost consciousness and assists in meeting budgetary targets
  • Represent the on-site laboratory in meetings as required by management
  • Communicate with study team, suppliers, Lab Manager or other stakeholders in a professional and effective manner
  • Comply with Good Clinical Practice (GCP) and standard operating procedures (SOPâ??s) in all lab duties, processes/ activities
  • Verify accuracy of data source documentation and accuracy of transcription from source data to Case Reports Forms (CRF) as needed
  • Ensure errors on source documents e.g. CRFâ??s are corrected, initialled and dated
  • Support the timely transmission/ data faxing or relevant Case Report Forms following QC activity (as needed)
  • Ensure completion of corrective action of internal and external QC reports and monitoring reviews
  • Perform quality control procedures as Lab SOPS and LQMP
  • Effectively communicate/ report all quality challenges to the Lab Manager
  • Ensure conformance to the External Quality Assurance program
  • Identify and communicate trends in quality of lab testing or control procedures
  • Assist with staff training (and retraining) where error trends are identified
  • Attend to audit reports and effectively implement corrective action and future preventative measures
  • Identify and develop new SOPs for new studies according to study protocols as per lab manager/project manager request
  • Review SOPs as required and ensure SOP file is updated
  • Ensure lab documentation filing is up to date and audi
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Executive Placements
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