Remote Clinical Research Associate – Global Trials

Placements24; Cape Town; Hybride; ZAR 500 000 - 800 000; Plein temps

Résumé du poste

Placements24 is seeking an experienced Remote Clinical Research Associate to join a global drug development team. You will monitor trial sites remotely, verify data, and ensure GCP compliance from your location.

The role emphasizes collaboration with investigators, site staff, and internal study teams to uphold data integrity and patient safety. Requirements include a life sciences-related bachelor's degree and 3+ years of CRA experience, with a regulatory-savvy mindset and strong organizational

Qualifications

• Minimum 3 years of CRA experience in clinical research.
• Thorough understanding of trial processes and GCP.
• Experience with remote monitoring tools.
• Proficient in CTMS and EDC systems.
• Eligible to work remotely in the designated region.

Responsabilités

• Conduct remote monitoring of trial sites to ensure protocol adherence.
• Verify data accuracy through remote SDV and data verification.
• Ensure compliance with GCP, FDA regulations, and guidelines.
• Maintain relationships with investigators and site staff.
• Identify risks and implement corrective actions at sites.
• Support site initiation, monitoring, and close-out activities.
• Submit timely monitoring reports and study documents.
• Participate in training to stay current with industry practices.
• Contribute to overall trial quality and patient safety.

Connaissances

Remote monitoring

SDV

GCP knowledge

CTMS

EDC systems

Data integrity

Regulatory knowledge

Time management

Communication

Independent work

Formation

Bachelor's degree

Master's degree

Outils

CTMS

EDC

Description du poste

Placements24 is seeking an experienced Remote Clinical Research Associate to join a global drug development team. You will monitor trial sites remotely, verify data, and ensure GCP compliance from your location.

The role emphasizes collaboration with investigators, site staff, and internal study teams to uphold data integrity and patient safety. Requirements include a life sciences-related bachelor's degree and 3+ years of CRA experience, with a regulatory-savvy mindset and strong organizational