Clinical Research Associate - Site Monitoring & Trials

Placements24; Centurion; Hybrid; ZAR 600,000 - 950,000; Full time

Benefits offered by this job

Health insurance

Life insurance

Disability coverage

Annual leave

Training opportunities

Work-life balance

Job summary

Placements24 in Centurion, Gauteng, is seeking a dedicated Clinical Research Associate to monitor sites, ensure data integrity, and uphold GCP standards.

You will perform site selection, initiation, monitoring, and close-out visits; manage CTMS and EDC systems; travel up to 50%; and collaborate with investigators and sponsors.

The ideal candidate holds a life sciences related degree, 3–5 years of CRA experience, and is familiar with ICH/GCP; certification such as ACRP/SoCRA is advantageous.

Qualifications

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
• 3–5 years of CRA experience in the pharmaceutical industry.
• In-depth understanding of GCP, ICH guidelines, and local regulatory requirements.
• Experience conducting site monitoring visits and managing multiple trials.

Responsibilities

• Conduct site monitoring visits (selection, initiation, monitoring, close-out) per GCP.
• Verify data integrity via source data verification and CRF reviews.
• Monitor patient safety and report adverse events.
• Ensure compliance with study protocol, regulations, and SOPs.
• Maintain strong relationships with investigators, site staff, and sponsors.
• Manage investigational product accountability and storage.

Skills

Communication skills

Interpersonal skills

Organizational skills

Attention to detail

Analytical skills

Education

Bachelor's degree in Life Sciences

Nursing

Pharmacy

Tools

CTMS

EDC systems

Job description

Placements24 in Centurion, Gauteng, is seeking a dedicated Clinical Research Associate to monitor sites, ensure data integrity, and uphold GCP standards.

You will perform site selection, initiation, monitoring, and close-out visits; manage CTMS and EDC systems; travel up to 50%; and collaborate with investigators and sponsors.

The ideal candidate holds a life sciences related degree, 3–5 years of CRA experience, and is familiar with ICH/GCP; certification such as ACRP/SoCRA is advantageous.