Hybrid Clinical Research Associate — Site Monitoring

Placements24; Rustenburg; Híbrido; ZAR 520.000 - 760.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Competitive salary

Medical, dental, vision benefits

Company car or travel allowance

Retirement fund contribution

Professional development opportunities

Flexible working arrangements

Descripción de la vacante

Placements24 seeks a diligent Clinical Research Associate to support clinical trials in the Rustenburg area with a hybrid work setup. You will monitor sites, review data, and ensure adherence to protocols, SOPs, and regulatory requirements, while coordinating with investigators and study teams.

The role requires a Life Sciences degree, at least 3 years of CRA experience, and strong GCP knowledge. Travel to sites and remote-task management are expected in this position.

Formación

• Bachelor's degree in Life Sciences or related field is required.
• Minimum 3 years of CRA or similar experience in clinical trials.
• Strong understanding of GCP and regulatory guidelines.

Responsabilidades

• Monitor clinical trial sites for protocol compliance and data integrity.
• Review source data and case report forms for accuracy and completeness.
• Communicate trial progress and issues with investigators and teams.
• Identify and resolve deviations or potential issues in trials.
• Ensure timely recruitment and adherence to timelines.
• Conduct site initiation, monitoring, and close-out visits as needed.

Conocimientos

GCP knowledge

Site monitoring

Regulatory compliance

Data management

Communication

Time management

Educación

Bachelor's degree in Life Sciences

Herramientas

CTMS

eCRF systems

Clinical trial software

Descripción del empleo

Placements24 seeks a diligent Clinical Research Associate to support clinical trials in the Rustenburg area with a hybrid work setup. You will monitor sites, review data, and ensure adherence to protocols, SOPs, and regulatory requirements, while coordinating with investigators and study teams.

The role requires a Life Sciences degree, at least 3 years of CRA experience, and strong GCP knowledge. Travel to sites and remote-task management are expected in this position.