Travel-Ready Clinical Research Associate (CRA)

Placements24; Willows (CA); On-site; USD 36,000 - 54,000; Full time

Benefits offered by this job

Competitive rate

Travel opportunities

Professional development

Exposure to diverse trials

Job summary

Placements24 seeks a meticulous Clinical Research Associate (CRA) to oversee site monitoring for trials in Welkom, Free State. The role emphasizes data integrity, patient safety, and protocol adherence. You will travel regularly to sites and ensure compliance with ICH-GCP and FDA guidelines.

The ideal candidate holds a life sciences degree, 3–5 years of CRA experience, and strong CTMS/EDC proficiency. Join a prominent pharmaceutical research organization committed to high standards and patient

Qualifications

• Bachelor’s degree in life science, nursing, pharmacy or related discipline.
• 3–5 years of direct CRA experience.
• Strong knowledge of clinical trials, ICH-GCP and regulatory affairs.
• Experience in site monitoring, data verification and regulatory compliance.
• Excellent written and verbal communication skills.
• Proficient in CTMS and EDC systems.
• Able to travel extensively within the region.

Responsibilities

• Conduct site selection, initiation, monitoring and close-out visits per protocols and SOPs.
• Verify data through SDV for accuracy and completeness.
• Monitor patient safety and adverse event reporting per regulations.
• Train site personnel on protocol requirements and data collection.
• Maintain communication between sponsor/CRO and trial sites.
• Ensure regulatory compliance with ICH-GCP, FDA and local guidelines.
• Prepare and submit site monitoring reports timely.
• Identify risks at sites and develop mitigation strategies.
• Oversee investigational product management and supplies at sites.
• Facilitate audits and inspections as required.
• Maintain organized site files and documentation.
• Contribute to successful trials in Welkom, Free State and surrounding areas.

Skills

Site Monitoring

CTMS

EDC

Data Integrity

ICH-GCP

Regulatory Compliance

Travel

Communication

Documentation

Education

Bachelor’s degree in life science

Tools

CTMS software

EDC systems

Job description

Placements24 seeks a meticulous Clinical Research Associate (CRA) to oversee site monitoring for trials in Welkom, Free State. The role emphasizes data integrity, patient safety, and protocol adherence. You will travel regularly to sites and ensure compliance with ICH-GCP and FDA guidelines.

The ideal candidate holds a life sciences degree, 3–5 years of CRA experience, and strong CTMS/EDC proficiency. Join a prominent pharmaceutical research organization committed to high standards and patient