Description

Clinical Trial Assistant (CTA)

Tiervlei Trial Centre · Cape Town · Full-time

Tiervlei Trial Centre is looking for a motivated and detail-oriented individual to join our team as a Clinical Trial Assistant. This is an entry-level position ideal for someone who is passionate about building a long-term career in clinical trials and the broader clinical research industry.

Minimum requirements

Grade 12 certificate (minimum)
Good administrative and computer skills (MS Word, Excel, Outlook)
Strong communication, organisational, and interpersonal skills
Honest, reliable, and able to work with attention to detail
A scientific degree (e.g. Physiology, Biomedical Sciences, Nursing, Pharmacy or related field) will be to your advantage
GCP certification advantageous but not required — training will be provided

Key responsibilities

Prepare, complete, and maintain accurate patient files and study/site files in line with protocol and regulatory requirements
Capture patient data on electronic data capture (EDC) systems accurately and timeously, and assist with query resolution
Order, prepare, receive, and control study materials and investigational products (IP) in accordance with SOPs
Prepare source documents and assist with study visit logistics and participant scheduling
Assist with archiving of study documentation and ensure all records are complete and audit-ready
Liaise professionally with monitors, sponsors, and study participants
Adhere to all study-specific protocols, SOPs, and GCP standards at all times

This role offers the opportunity to learn and grow within a professional clinical research environment.

Please send your resume/CV