Remote CRA — Trial Monitoring & Data Integrity

Placements24; Centurion; Hybrid; ZAR 480,000 - 640,000; Full time

Benefits offered by this job

Competitive rate

Diverse therapeutic areas

Contract extension

Remote work with site visits

Job summary

Placements24 is seeking a motivated Clinical Research Associate (CRA) on a contract basis to support pharmaceutical studies in the Centurion area and surroundings. You will monitor trial sites, ensure adherence to protocols, and safeguard patient safety and data integrity.

You will travel as required, conduct SDV, and maintain TMF, collaborating with investigators and staff to drive compliant, high-quality trials across therapeutic areas.

Qualifications

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or related discipline.
• Minimum of 3 years of CRA experience in pharma/biotech.
• Strong knowledge of GCP, ICH guidelines and regulatory frameworks.
• Proven ability to conduct site monitoring visits effectively.
• Excellent communication, interpersonal and organizational skills.
• Willingness to travel extensively to clinical trial sites.

Responsibilities

• Conduct site initiation, interim monitoring and close-out visits.
• Perform source data verification to ensure data accuracy.
• Ensure compliance with GCP, ICH, and study protocols.
• Maintain strong relationships with investigators and site staff.
• Identify and report deviations, adverse events, or safety concerns.
• Manage TMF and site documents.

Skills

Communication skills

Site monitoring

Regulatory compliance

Travel readiness

Education

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

Job description

Placements24 is seeking a motivated Clinical Research Associate (CRA) on a contract basis to support pharmaceutical studies in the Centurion area and surroundings. You will monitor trial sites, ensure adherence to protocols, and safeguard patient safety and data integrity.

You will travel as required, conduct SDV, and maintain TMF, collaborating with investigators and staff to drive compliant, high-quality trials across therapeutic areas.