Oncology Clinical Research Associate - Hybrid Role

Placements24; Centurion; Hybrid; ZAR 550,000 - 900,000; Full time

Benefits offered by this job

Medical aid

Provident fund

Life insurance

Job summary

Placements24 seeks an experienced Clinical Research Associate (Oncology) to monitor study sites, verify patient records, and ensure strict adherence to protocols and regulatory standards. The role blends on-site monitoring with remote reporting and administration from Centurion, South Africa.

The ideal candidate has 3–5 years in oncology-focused CRA roles, strong GCP knowledge, and excellent communication skills to collaborate with investigators and site staff.

Qualifications

• Bachelor’s degree in a life science, nursing, or related field.
• 3–5 years of CRA experience with a focus on oncology trials.
• Strong understanding of GCP and regulatory requirements (ICH, FDA, EMA, SAHPRA).
• Experience in site monitoring, data review, and query resolution.

Responsibilities

• Conduct site initiation, routine monitoring, and close-out visits per protocols and GCP.
• Verify data accuracy by reviewing source documents and CRFs.
• Manage data queries and maintain data integrity.
• Assess site staff adherence to protocols and consent procedures.
• Serve as primary contact for assigned sites and build investigator relationships.
• Ensure investigational product management and drug dispensing at sites.
• Identify risks at sites and implement mitigation strategies.
• Prepare monitoring reports and follow-up on actions.
• Maintain knowledge of oncology treatments and trial regulations.

Skills

Oncology trials

Site monitoring

GCP compliance

Data query resolution

Excellent communication

Travel up to 50%

Education

Bachelor's degree in life science or nursing

Tools

EDC systems

Clinical trial management software

Job description

Placements24 seeks an experienced Clinical Research Associate (Oncology) to monitor study sites, verify patient records, and ensure strict adherence to protocols and regulatory standards. The role blends on-site monitoring with remote reporting and administration from Centurion, South Africa.

The ideal candidate has 3–5 years in oncology-focused CRA roles, strong GCP knowledge, and excellent communication skills to collaborate with investigators and site staff.