At a Glance
- Tasks: Oversee clinical studies, ensuring compliance and supporting data integrity.
- Company: The Origin Group Ltd, a leading firm in clinical research.
- Benefits: 25 days holiday, pension contribution, and a supportive work environment.
- Other info: Opportunity to work independently in a dynamic and impactful role.
- Why this job: Make a difference in clinical research while ensuring participant safety.
- Qualifications: Minimum three years in clinical research monitoring and strong ICH-GCP knowledge.
The predicted salary is between 40000 - 48822 £ per year.
The Origin Group Ltd in Cambridge is seeking a Study Monitor / Clinical Research Associate to oversee clinical studies.
This role involves ensuring compliance with the protocol, monitoring sites, and supporting data integrity.
Ideal candidates will have a minimum of three years in clinical research monitoring, a strong understanding of ICH-GCP, and the ability to work independently while ensuring participant safety.
The position includes benefits like 25 days holiday and a pension contribution.
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Remote Clinical Research Associate - Monitoring & Compliance in Cambridge employer: Website
The Origin Group Ltd is an exceptional employer located in the vibrant city of Cambridge, offering a supportive work culture that prioritises employee well-being and professional growth. With generous benefits such as 25 days of holiday and a pension contribution, we foster an environment where clinical research professionals can thrive while making a meaningful impact on participant safety and data integrity.
