As a Clinical Trials Assistant, you will be at the forefront of our research efforts in Pretoria. You will be key in data entry, tracking patient visits, and coordinating between participants and clinical staff.
Responsibilities
Ensure ethical compliance and subject confidentiality in trials.
Document site and trial-related activities and findings.
Assist in training and onboarding new team members.
Support the preparation of reports for regulatory agencies.
Facilitate team meetings and ensure proper follow-up on action items.
Contribute to continuous improvement of clinical processes.
Requirements
Education
Bachelor's or Master's degree in Biomedical Sciences or related field
Experience
2+ years of experience in clinical trial assistance or coordination roles
Technical Skills
Electronic Data Capture (EDC) Systems
Project Management
Soft Skills
Problem-solving
Teamwork
Advantageous
Experience in patient interaction or support: Experience in direct interactions with study participants.
Knowledge of biostatistics: Exposure to biostatistical methods and applications in trials.
Benefits
Comprehensive health and wellness programs
Flexible working hours
Support for further education and certifications
Work-life balance initiatives
Company Culture
Inclusivity in Research: We celebrate diversity and strive for inclusivity in all aspects of our work.
Focused on Results: Results-driven approach with emphasis on achieving impactful outcomes.
Team-oriented Atmosphere: A supportive culture that values teamwork and shared success.