About the job
The Clinical Research Associate (CRAII - CRAIII) plays a vital role in protecting the rights and wellbeing of trial participants while ensuring the accuracy and completeness of trial data. This job offers a fantastic opportunity to work in a supportive environment that values work-life balance and inclusivity. Team members are encouraged to thrive in their careers while enjoying flexible working arrangements and a commitment to professional development.
You'll be responsible for
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Building relationships
Establishing and maintaining strong relationships with Principal Investigators, study coordinators, and site personnel to ensure smooth trial management.🔍
Monitoring investigational sites
Conducting monitoring visits across all phases of clinical trials to ensure compliance with ICH GCP and study requirements.🚀
Driving site recruitment initiatives
Developing and executing site-specific recruitment plans to meet participant targets and enhance engagement.Key criteria
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Graduate in clinical or life sciences
Possess a degree in a relevant field for foundational knowledge.View
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CRA II: 6+ months monitoring experience
Demonstrated independent monitoring experience in clinical trials.View
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CRA III: 2+ years monitoring experience
Proven independent monitoring experience in clinical research.View
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