Hybrid CRA - Trials Monitoring in Soweto

Placements24; Soweto; Hybrid; ZAR 600,000 - 900,000; Full time

Benefits offered by this job

Competitive salary package

Medical, dental, and vision insurance

Retirement savings plan

Generous paid time off

Professional development opportunities

Hybrid role based in Soweto

Job summary

Placements24 is seeking a Pharmaceutical Clinical Research Associate for a hybrid role based in Soweto, Gauteng. You will monitor clinical trials, review data, and ensure adherence to GCP and regulatory standards, while traveling to sites as needed.

The ideal candidate has a life sciences degree and 3–5 years of CRA experience, with strong documentation and communication skills to support site staff and investigators.

Qualifications

• Bachelor’s degree in life science, nursing, pharmacy, or related field.
• 3–5 years of experience as a CRA or similar monitoring role.
• Strong knowledge of GCP, ICH guidelines, and regulatory requirements.
• Experience with site monitoring, data review, and query resolution.
• Ability to travel regularly to trial sites.

Responsibilities

• Conduct site visits to monitor trial progress and ensure protocol compliance.
• Verify accuracy of trial data via source data verification.
• Ensure patient safety and GCP/regulatory adherence.
• Train and support site staff on procedures and compliance.
• Maintain essential trial documents and proper filing.
• Prepare and submit monitoring reports in a timely manner.
• Oversee regulatory, safety, and quality aspects at sites.

Skills

Clinical research

GCP/ICH knowledge

Site monitoring

Travel-ready

Documentation skills

Education

Bachelor's degree in life science/ nursing/ pharmacy/ related field

Tools

CTMS

EDC

Job description

Placements24 is seeking a Pharmaceutical Clinical Research Associate for a hybrid role based in Soweto, Gauteng. You will monitor clinical trials, review data, and ensure adherence to GCP and regulatory standards, while traveling to sites as needed.

The ideal candidate has a life sciences degree and 3–5 years of CRA experience, with strong documentation and communication skills to support site staff and investigators.