CRA II - Site Monitoring & Data Integrity Expert

Placements24; Kempton Park; On-site; ZAR 520,000 - 760,000; Full time

Benefits offered by this job

Health insurance

Life insurance

Retirement fund contribution

Paid time off

Professional development

Job summary

Placements24 in South Africa seeks an experienced Clinical Research Associate II to oversee monitoring of trials, ensure data integrity, and uphold GCP standards at trial sites in Gauteng. This role emphasizes collaboration with investigators and staff to drive patient safety and protocol adherence.

The successful candidate will have a life sciences degree, 3–5 years as CRA, strong documentation and CTMS/EDC proficiency, and willingness to travel up to 60% to sites.

Qualifications

• Bachelor's degree in life science, nursing or related discipline.
• 3–5 years of CRA experience with monitoring trials.
• Knowledge of GCP, ICH and regulatory requirements.
• Experience in site monitoring visits and managing CRFs/TMFs.
• Excellent organizational and communication skills.
• Ability to travel up to 60%.
• Proficient in CTMS and EDC systems.
• Ability to work independently and in a team.
• Attention to detail and data quality.

Responsibilities

• Conduct site selection, initiation, monitoring, and close-out visits per GCP.
• Ensure trials are conducted, recorded, and reported per protocol and SOPs.
• Verify accuracy and integrity of data via source and CRFs.
• Manage trial master files and essential study docs.
• Communicate study progress with investigators and teams.
• Identify, track, and resolve site issues promptly.
• Ensure subject safety and protocol compliance at sites.
• Prepare and present monitoring visit reports and actions.
• Participate in investigator meetings and training.

Skills

GCP knowledge

Site monitoring

Regulatory compliance

Documentation

CTMS/EDC

Travel availability

Education

Bachelor's degree in life sciences

Tools

CTMS

EDC systems

Job description

Placements24 in South Africa seeks an experienced Clinical Research Associate II to oversee monitoring of trials, ensure data integrity, and uphold GCP standards at trial sites in Gauteng. This role emphasizes collaboration with investigators and staff to drive patient safety and protocol adherence.

The successful candidate will have a life sciences degree, 3–5 years as CRA, strong documentation and CTMS/EDC proficiency, and willingness to travel up to 60% to sites.