Senior Clinical Research Associate - Phase III Monitoring

Placements24; Kempton Park; Sur place; ZAR 600 000 - 900 000; Plein temps

Avantages offerts par ce poste

Competitive salary

Travel allowance

Health, wellness & life insurance

Retirement fund contribution

Career advancement

Ongoing training & professional dev.

Per diem for overnight travel

Company mobile phone and laptop

Résumé du poste

Placements24 is seeking a dedicated Clinical Research Associate (CRA) to join their expanding clinical operations team in South Africa. This field-based role monitors trial sites, ensures data integrity, and verifies regulatory compliance for Phase III studies.

The successful candidate will travel up to 70% across Tembisa, Gauteng and surrounding areas, hold a Life Sciences degree, at least 3 years of CRA experience, and be proficient with GCP/ICH and EDC systems.

Qualifications

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related healthcare field.
• Minimum of 3 years of direct CRA experience with significant exposure to Phase III trials.
• In-depth knowledge of Good Clinical Practice (GCP), ICH guidelines, and regulatory requirements.
• Proven experience in site monitoring, data verification, and query resolution.

Responsabilités

• Conduct on-site visits to investigational sites to monitor progress, data accuracy, and compliance with protocols, SOPs, and GCP.
• Verify source documentation against case report forms (CRFs) to ensure data integrity.
• Train site staff on study procedures, regulatory requirements, and data collection processes.
• Manage and resolve data queries in a timely and efficient manner.
• Ensure all study-related documentation is maintained accurately and securely at the site and in the trial master file.
• Identify, report, and escalate any deviations, potential risks, or adverse events to the clinical trial manager.
• Build and maintain strong working relationships with investigators and site personnel.
• Participate in investigator meetings and provide updates on site performance.
• Contribute to the development and review of study protocols and other essential documents.

Connaissances

Site monitoring

Data verification

Travel readiness

GCP/ICH knowledge

Communication skills

Formation

Bachelor's degree in Life Sciences/Nursing/Pharmacy

Outils

EDC systems

Description du poste

Placements24 is seeking a dedicated Clinical Research Associate (CRA) to join their expanding clinical operations team in South Africa. This field-based role monitors trial sites, ensures data integrity, and verifies regulatory compliance for Phase III studies.

The successful candidate will travel up to 70% across Tembisa, Gauteng and surrounding areas, hold a Life Sciences degree, at least 3 years of CRA experience, and be proficient with GCP/ICH and EDC systems.