Clinical Research Associate

Placements24; Cape Town; On-site; ZAR 600,000 - 900,000; Full time

Benefits offered by this job

Medical aid

Retirement plan

Travel opportunities

Career growth

Supportive team

Job summary

Placements24 seeks a meticulous and experienced Clinical Research Associate (CRA) to join the clinical operations team in Cape Town. You will oversee site monitoring, data verification, and ensure adherence to protocols and regulatory standards.

The ideal candidate has a life sciences degree, CRA experience, and strong knowledge of ICH-GCP. Excellent organizational and communication skills are essential for collaborating with investigators and study staff.

Qualifications

• Bachelor's degree in life sciences or related field; advanced degree preferred.
• Experience as a CRA in pharma/biotech environments.
• Knowledge of ICH-GCP guidelines and regulatory submissions.
• Excellent organizational and communication skills, with Cape Town-specific collaboration in mind.

Responsibilities

• Conduct on-site and remote monitoring visits to verify data accuracy and protocol compliance.
• Ensure compliance with GCP and regulatory requirements.
• Manage investigational product accountability and handling.
• Build relationships with investigators and site staff, providing training and support.
• Prepare monitoring reports and recommend corrective actions to keep trials on track.

Skills

Site monitoring

GCP/ICH

Data verification

Regulatory submissions

Communication

Training investigators

Education

Bachelor's degree in life sciences

Tools

CTMS

EDC

Job description

About the Role

Our client is seeking a meticulous and experienced Clinical Research Associate (CRA) to join their dedicated clinical operations team in Cape Town . This role is crucial for overseeing and managing clinical trials, ensuring adherence to protocols, regulatory standards, and ethical guidelines. You will be responsible for site monitoring, data verification, and maintaining effective communication with investigators, study staff, and internal project teams. The position requires a strong commitment to data integrity and patient safety within the vibrant research landscape of the Western Cape .

Key Responsibilities

• Conduct on-site and remote monitoring visits to clinical trial sites to verify data accuracy and protocol compliance.
• Ensure compliance with Good Clinical Practice (GCP) and all applicable regulatory requirements.
• Manage investigational product accountability and ensure proper storage and handling.
• Build and maintain strong relationships with investigators and site staff, providing necessary training and support.
• Prepare and present monitoring reports, identifying potential issues and recommending corrective actions to ensure trial progress.

Requirements

• Bachelor's degree in a life science, nursing, or related field; advanced degree preferred.
• Proven experience as a Clinical Research Associate or similar role in the pharmaceutical or biotechnology industry.
• In-depth knowledge of clinical trial processes, ICH-GCP guidelines , and regulatory submissions.
• Excellent organizational, time management, and problem-solving skills.
• Strong communication and interpersonal abilities, with a focus on working effectively in Cape Town .

Benefits

• Competitive annual salary commensurate with experience.
• Comprehensive medical aid, retirement fund, and insurance benefits.
• Opportunities for career advancement within a growing organization.
• Travel opportunities for site visits and conferences.
• A supportive team environment committed to advancing medical research in South Africa .