About the Role

We are looking for a detail-oriented Clinical Trial Assistant to support the planning, coordination, and administration of clinical research studies. You will work closely with clinical research teams to ensure trials are conducted efficiently, ethically, and in compliance with regulatory requirements.

What You'll Do

Assist with the coordination and administration of clinical trials
Prepare, organise, and maintain study documentation and trial records
Support study start-up, participant recruitment, and site management activities
Ensure clinical trial files are accurate, complete, and up to date
Coordinate meetings, schedules, and communications with research sites and sponsors
Track study progress and assist with regulatory submissions
Ensure compliance with Good Clinical Practice (GCP), study protocols, and regulatory guidelines
Assist with data entry, reporting, and trial documentation

Requirements

Degree or Diploma in Life Sciences, Nursing, Pharmacy, Clinical Research, or a related field
Previous experience in clinical research or healthcare is advantageous
Knowledge of Good Clinical Practice (GCP) and clinical trial processes is preferred
Strong organisational and administrative skills
Excellent attention to detail and communication abilities
Proficiency in Microsoft Office and clinical trial management systems is advantageous

Key Skills

✔ Clinical Trial Coordination

✔ Clinical Documentation

✔ Good Clinical Practice (GCP)

✔ Regulatory Compliance

✔ Data Entry & Reporting

✔ Organisation & Time Management

✔ Communication Skills