Field CRA: Clinical Trials in Richards Bay

Placements24

Richards Bay

Vor Ort

ZAR 550.000 - 800.000

Vollzeit

Vor 5 Tagen
Sei unter den ersten Bewerbenden

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

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Benefits dieser Stelle

Health insurance
Company car
Travel allowances

Zusammenfassung

Placements24 is seeking a dedicated Clinical Research Associate to oversee trials in Richards Bay, KwaZulu-Natal. This field-based role focuses on site monitoring, data quality, and regulatory compliance to support life-saving medicines.

The CRA will conduct site visits, SDV, training, and communication with investigators, travel extensively, and work with cross-functional teams to ensure study timelines are met and data integrity is maintained.

Qualifikationen

  • Bachelor's degree in life science, nursing, pharmacy, or related field.
  • Minimum of 3 years' CRA experience in pharma.
  • Solid knowledge of GCP/ICH and regulatory requirements.
  • Experience with SDV and site monitoring.
  • Strong communication and travel readiness.

Aufgaben

  • Perform site selection, initiation, monitoring, and close-out visits.
  • Verify data via source data verification and ensure data integrity.
  • Ensure adherence to protocols, GCP, and regulatory requirements.
  • Train and support site staff on procedures and data collection.
  • Coordinate with project teams to keep trials on track.
  • Monitor patient recruitment and site performance.
  • Maintain drug accountability and site communications.

Kenntnisse

GCP knowledge
ICH guidelines
Site monitoring
SDV
EDC systems
Data management
Communication

Ausbildung

Bachelor's degree in life science/related field

Tools

EDC systems
Clinical trial management software
Regulatory documentation

Jobbeschreibung

Placements24 is seeking a dedicated Clinical Research Associate to oversee trials in Richards Bay, KwaZulu-Natal. This field-based role focuses on site monitoring, data quality, and regulatory compliance to support life-saving medicines.

The CRA will conduct site visits, SDV, training, and communication with investigators, travel extensively, and work with cross-functional teams to ensure study timelines are met and data integrity is maintained.

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