At a Glance
- Tasks: Monitor clinical studies, ensuring data integrity and participant safety.
- Company: The Origin Group Ltd, a leader in clinical research.
- Benefits: Flexible working options, competitive salary, and professional development opportunities.
- Other info: Dynamic role with opportunities for growth and learning.
- Why this job: Make a real difference in clinical research while building strong relationships.
- Qualifications: Experience in clinical research and strong communication skills.
The predicted salary is between 40000 - 50000 £ per year.
The Origin Group Ltd (TOGL) is seeking a Study Monitor / Clinical Research Associate to monitor clinical studies in line with the approved protocol, GCP and sponsor SOPs.
You will provide oversight of study sites, ensure data integrity and participant safety, and support audits and CAPA processes.
The role reports to the Head of Clinical Operations and involves both on-site and remote monitoring across UK-based studies, building strong relationships with site teams and internal stakeholders.
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Clinical Research Associate - Site Monitoring & Data Integrity in Cambridge employer: Origin Sciences
The Origin Group Limited (TOGL) is an exceptional employer, offering a dynamic work environment that fosters innovation in the medical technology sector. With a strong commitment to employee growth, TOGL provides opportunities for professional development and encourages collaboration among teams dedicated to improving patient outcomes. Located in the UK, employees benefit from a supportive culture, competitive salaries, and a generous holiday allowance, making it an ideal place for those seeking meaningful and rewarding careers in clinical research.
