Clinical Trials Specialist

2 weeks ago


London, Greater London, United Kingdom UCL Eastman Dental Institute Full time
About the Role

The Pharmacovigilance Officer will be a key member of the CTC Regulatory team, working closely with all staff at UCL Eastman Dental Institute. With the support of the PV Manager, the main purpose of the post is to maintain oversight of safety reporting activities within the CTC, ensuring patient safety and compliance with regulatory requirements are maintained at all times.

The post-holder will need to maintain familiarity with all current legislation and guidelines relevant to pharmacovigilance in clinical trials (pregnancy, AE/SAE reporting, etc.), advanced therapies and non-drug interventions.

We offer a competitive salary of £45,000 - £55,000 per annum, depending on experience, as well as a range of benefits including flexible working, hybrid working, and opportunities for professional development.

About You

You will have significant knowledge of biomedical or life sciences, experience of handling data, in particular safety data in relation to clinical trials and familiarity with current regulatory requirements governing clinical trials.



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