Kimberley CRA: Site Monitoring & Data Integrity

Placements24; Noord-Kaap; Hybrid; ZAR 600,000 - 900,000; Full time

Benefits offered by this job

Medical benefits

Retirement benefits

Travel allowances

Paid time off

Professional development

Exposure to cutting-edge research

Job summary

Placements24 is seeking a diligent Pharmaceutical Clinical Research Associate (CRA) to join a renowned pharma company serving the Kimberley, Northern Cape region. You will monitor and support clinical trial sites, ensuring adherence to GCP, protocols, and regulatory requirements.

The role involves site initiation, routine monitoring visits, data verification, safety assessments, and training site staff. Travel within Kimberley and surrounding areas is expected, and you will collaborate with

Qualifications

• Bachelor's degree in Nursing, Pharmacy, Life Sciences, or related field.
• 3–5 years of CRA or equivalent experience.
• Strong knowledge of GCP/ICH guidelines.
• Experience in site monitoring and regulatory documentation.
• Excellent organizational and communication skills.
• Willingness to travel within Kimberley region.

Responsibilities

• Conduct feasibility, initiation, monitoring, and close-out visits.
• Ensure compliance with study protocols, SOPs, GCP, and regulations.
• Verify data accuracy by reviewing source documents and CRFs.
• Assess patient safety and eligibility.
• Train site staff on procedures.
• Act as liaison between sites and study team.
• Resolve data queries and ensure timely entry.
• Manage regulatory documents and site files.
• Prepare monitoring reports and communicate findings.
• Support timely patient recruitment.

Skills

GCP knowledge

Data verification

Regulatory documentation

Travel ready

Communication skills

Education

Bachelor's degree in Nursing, Pharmacy, Life Sciences, or related field

Tools

EDC systems

CTMS

Source data review tools

Job description

Placements24 is seeking a diligent Pharmaceutical Clinical Research Associate (CRA) to join a renowned pharma company serving the Kimberley, Northern Cape region. You will monitor and support clinical trial sites, ensuring adherence to GCP, protocols, and regulatory requirements.

The role involves site initiation, routine monitoring visits, data verification, safety assessments, and training site staff. Travel within Kimberley and surrounding areas is expected, and you will collaborate with