Clinical Trial Assistant (CTA) - Research Support

Placements24; Noord-Kaap; On-site; ZAR 180,000 - 280,000; Full time

Job summary

Placements24 is seeking a detail-oriented Clinical Trial Assistant (CTA) in Kimberley, Northern Cape to provide essential administrative support for ongoing clinical trials. You will help with document management, participant scheduling, data entry and regulatory file preparation in a fast-paced research environment.

This entry-level role offers hands-on experience in clinical research, supporting Clinical Research Coordinators and Monitors while contributing to timely and compliant study

Qualifications

• Entry-level opportunity for individuals starting a career in pharmaceutical research.
• Strong organizational and communication skills are essential.
• Ability to work with clinical trial documentation and regulatory files.

Responsibilities

• Provide administrative and operational support for ongoing clinical trials.
• Assist with document management, participant scheduling, data entry and regulatory file preparation.
• Support Clinical Research Coordinators and Monitors to ensure trial timelines are met.

Skills

Document management

Data entry

Scheduling coordination

Communication skills

Job description

About the Role

Our client is looking for a detail-oriented Clinical Trial Assistant (CTA) to provide essential administrative and operational support for ongoing clinical trials in Kimberley, Northern Cape. This role is crucial for the smooth execution of clinical research activities, ensuring that all study documentation is maintained accurately and that trial timelines are met. The CTA will assist Clinical Research Coordinators and Monitors with tasks such as document management, participant scheduling, data entry, and regulatory file preparation. This is an excellent entry-level opportunity for individuals looking to build a career in the pharmaceutical research sector. You will gain hands-on experience in a clinical research environment and contribute directly to the success of important medical studies. The position requires strong organizational skills, excellent communication, and a proactive attitude towards supporting the research team. We are dedicated to providing a supportive environment for professional development and career growth within clinical research operations.