Manufacturing

Project Coordinator (clinical Trials) | Centurion

Ampath·Gauteng, south-africa·Full Time·Contract
ManufacturingFull TimeContract
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What You Will Do (Role Impact)

Ensure Accurate Data Management and Operational Excellence

  • Handle patient reports and related administration to ensure accurate, timely, and effective reporting of patient data.
  • Build and maintain positive client relationships that enhance the reputation and service excellence of Ampath.
  • Support Project Managers by reviewing test runs and assisting with the correct setup and execution of clinical studies.
  • Prepare documentation and data for raw data audits and provide support during audit processes to ensure compliance requirements are met.
  • Assist with additional operational requests and tasks to support workflow efficiency and departmental objectives.
  • Monitor ACT storage facilities, including fridges, freezers, and room monitoring systems, to ensure compliance with temperature and storage requirements.

Provide Administrative and Project Support

  • Perform general administrative duties to support departmental operations and team effectiveness.
  • File, maintain, archive, and retrieve documents to ensure efficient record management and data accessibility.
  • Assist with kit-building activities as required to support study preparation and operational needs.

Qualifications

Required

  • Grade 12.

Advantageous

  • Completed GCP, GLP, or GCLP certification.

Experience

  • 4 or more years' experience in administration, client services, or data capturing, preferably within a pathology, laboratory, healthcare, or clinical trials environment.

Knowledge and Skills

  • Strong computer literacy and the ability to use technology effectively in a professional environment.
  • Excellent verbal and written communication skills in English.
  • Sound numerical reasoning skills, including basic calculations and percentage-based computations.
  • High attention to detail and a strong commitment to accuracy and quality.
  • Strong interpersonal and relationship-building skills with the ability to collaborate effectively across diverse stakeholder groups.
  • Working knowledge of Good Laboratory Practice (GLP) principles and quality requirements.
  • Ability to maintain strict confidentiality and exercise discretion when handling sensitive information and records.
  • Strong organisational and time management skills with the ability to manage multiple priorities.

Key skills

Matric

At a glance

Company

Ampath

Location

Gauteng, south-africa

Employment

Full Time

Experience

Valid until

Not specified

Created

October 16, 2026