Clinical Research Associate - George

Placements24; George; Hybrid; ZAR 420,000 - 660,000; Full time

Benefits offered by this job

Competitive salary

Health insurance

Company vehicle or travel allowance

Generous paid time off

Professional development

Job summary

Placements24 is seeking a meticulous Clinical Research Associate to join the clinical operations team in the George region. You will monitor trial sites, verify data, ensure patient safety, and uphold GCP compliance throughout study conduct.

The role requires a life sciences degree, at least two years as CRA or similar, and strong knowledge of ICH-GCP, EDC, and CTMS. Willingness to travel to sites in George and surrounding areas is essential.

Qualifications

• Bachelor’s degree in life science, nursing, or related field.
• Minimum of 2 years of experience as a CRA or similar role.
• In-depth knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials.
• Experience with EDC systems and CTMS.
• Excellent organizational, problem-solving, and communication skills.
• Willingness to travel to George region and surrounding areas.

Responsibilities

• Conduct site visits (initiation, interim, and close-out) to ensure compliance with protocols, regulations, and SOPs.
• Verify the accuracy, completeness, and integrity of clinical trial data through source data verification.

Skills

Attention to detail

Communication

Problem-solving

Travel readiness

Education

Bachelor's degree in life sciences

Tools

EDC systems

CTMS

Job description

About the Role

Our client is looking for a meticulous and dedicated Clinical Research Associate (CRA) to join their clinical operations team, based in or covering the George region. This role is integral to ensuring the successful execution of clinical trials, adhering to strict protocols and regulatory standards. You will be responsible for monitoring clinical trial sites, verifying data accuracy, ensuring patient safety, and maintaining compliance with Good Clinical Practice (GCP) guidelines. This is an exciting opportunity to be at the forefront of medical innovation, working on cutting-edge research that aims to improve patient outcomes, within a company that values scientific integrity and professional growth.

Key Responsibilities

• Conduct site visits (initiation, interim, and close-out) to ensure compliance with protocols, regulations, and SOPs.
• Verify the accuracy, completeness, and integrity of clinical trial data through source document verification.
• Monitor patient safety and report adverse events according to regulatory requirements and study protocols.
• Train and support investigators and study site staff on trial procedures and requirements.
• Liaise with investigators, study coordinators, and other site personnel to resolve data queries.
• Ensure timely submission of essential documents and study supplies to the sites.

Requirements

• Bachelor's degree in a life science, nursing, or related scientific field.
• Minimum of 2 years of experience as a Clinical Research Associate or similar role.
• In-depth knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials.
• Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
• Excellent organizational, problem-solving, and communication skills.
• Ability to travel frequently to clinical trial sites within the George area and surrounding regions.

Benefits

• Competitive annual salary and performance-based bonuses.
• Comprehensive health, dental, and vision insurance.
• Company vehicle or travel reimbursement for site visits.
• Generous paid time off and holidays.
• Opportunities for professional development and certifications in clinical research.