Senior CRA – Site Monitoring & Trials (Rustenburg)

Placements24; Rustenburg; Híbrido; ZAR 550 000 - 850 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Health insurance

Retirement fund

Travel allowances

Training programs

Performance-based incentives

Resumo da oferta

Placements24 seeks a meticulous Clinical Research Associate (CRA) to join our client’s expanding team in Rustenburg, North West. The CRA will monitor trial sites, ensure data integrity, and uphold patient safety throughout the trial lifecycle.

The role requires 3–5 years of CRA experience, strong knowledge of GCP/ICH guidelines, and proficiency with CTMS/EDC systems. Travel to sites will be required as needed.

Qualificações

• Bachelor's degree in Life Sciences or related field required.
• GCP/ICH guidelines knowledge essential.
• Experience monitoring clinical trials (CRA) in pharma/CRO preferred.
• Strong organizational and communication skills required.
• Willingness to travel to trial sites.

Responsabilidades

• Monitor clinical trial sites for protocol and SOP compliance.
• Conduct site initiation, monitoring, and closure visits.
• Verify data via source data verification (SDV).
• Resolve data queries and discrepancies promptly.
• Oversee patient safety and AE/SAE reporting.

Conhecimentos

GCP/ICH knowledge

Site monitoring

Data integrity

Communication

Problem solving

Formação académica

Bachelor's degree in Life Sciences or related field

Master's degree (advantage)

Ferramentas

CTMS

EDC systems

Descrição da oferta de emprego

Placements24 seeks a meticulous Clinical Research Associate (CRA) to join our client’s expanding team in Rustenburg, North West. The CRA will monitor trial sites, ensure data integrity, and uphold patient safety throughout the trial lifecycle.

The role requires 3–5 years of CRA experience, strong knowledge of GCP/ICH guidelines, and proficiency with CTMS/EDC systems. Travel to sites will be required as needed.