Senior CRA — Site Monitoring & Data Quality

Placements24; Randburg; Híbrido; ZAR 600 000 - 900 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Health benefits

Bonuses

Career development opportunities

Resumo da oferta

Placements24 is seeking a Senior Clinical Research Associate to join our Randburg-based team to ensure trials comply with GCP and regulatory requirements.

You will monitor sites, manage data, train staff, and collaborate with investigators while supporting ongoing trial operations and quality assurance.

This role offers exposure to diverse therapeutic areas, a professional development track, and competitive benefits in a dynamic CRO setting.

Qualificações

• Bachelor's degree in life science, nursing, or related healthcare field.
• 4–5 years of CRA experience in pharma or CRO settings.
• In-depth knowledge of ICH-GCP and relevant regulations.
• Proven experience monitoring trials across multiple therapeutic areas.
• Strong site and data management understanding.
• Excellent organizational and communication skills.

Responsabilidades

• Conduct site initiation, routine monitoring, and close-out visits per protocol and GCP.
• Verify data accuracy by reviewing CRFs and source documents.
• Maintain strong relationships with investigators and study staff.
• Ensure timely submission of essential documents and drug accountability.
• Identify deviations and escalate risks to project management.
• Assist in study document preparation and monitoring plan development.
• Train site personnel on procedures and data collection.
• Participate in investigator meetings and teleconferences.
• Contribute to risk-based monitoring strategies.

Conhecimentos

ICH-GCP knowledge

Site monitoring

Communication skills

Travel readiness

Formação académica

Bachelor's degree in life science, nursing, or related healthcare field

Ferramentas

CTMS

EDC systems

Descrição da oferta de emprego

Placements24 is seeking a Senior Clinical Research Associate to join our Randburg-based team to ensure trials comply with GCP and regulatory requirements.

You will monitor sites, manage data, train staff, and collaborate with investigators while supporting ongoing trial operations and quality assurance.

This role offers exposure to diverse therapeutic areas, a professional development track, and competitive benefits in a dynamic CRO setting.