We are searching for a Medical and Clinical Laboratory Technologist with a solid understanding of clinical research protocols. This role involves monitoring clinical trials and ensuring adherence to regulatory guidelines.
Responsibilities
Monitor clinical trials to guarantee compliance with protocol, ICH, GCP, and applicable regulations.
Ensure timely and accurate data collection and reporting while coordinating site study activities.
Assist in study start-up, site initiation, and close-out activities.
Perform regular site visits, including site selection and ongoing monitoring.
Conduct training on protocol and study procedures for site staff.
Requirements
Education
Bachelor's degree in a healthcare-related discipline
Certification as a Clinical Research Associate (CRA) is advantageous
Experience
Minimum of 2 years' experience in clinical research
Technical Skills
Electronic Data Capture (EDC) systems
Clinical trial management systems (CTMS)
Soft Skills
Excellent communication
Time management
Languages
English: Fluent
Advantageous
Experience with oncology or infectious diseases trials: Prior involvement with specialized clinical trials for improved patient care.
Experience working on global studies: Familiarity with international protocols and multi-site clinical research.
Benefits
Competitive salary range of R300,000 – R600,000 per annum.
Health, dental, and vision insurance coverage.
Flexible working hours and the possibility for remote work.
Employee wellness programs to support a healthy work-life balance.
Company Culture
Collaboration: We foster a collaborative environment that values contributions from every team member.
Innovation: We encourage creative problem-solving and embrace novel approaches to research.
Diversity and Inclusion: We are committed to building a diverse team and welcoming applications from all backgrounds.