Location: | London, Hybrid |
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Salary: | £51,474 to £60,521 |
Hours: | Full Time |
Contract Type: | Permanent |
Placed On: | 17th July 2024 |
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Closes: | 26th July 2024 |
Job Ref: | B02-07216 |
About the role
The main purpose of this role is to ensure that all CTC trials are conducted in accordance with relevant regulatory and legislative requirements.
In particular the post holder is responsible for maintaining and overseeing:
• The Quality Management System (QMS) at the CTC, including the portfolio of standard operating procedures (SOPs) and programme of internal audits.
• Trial monitoring and oversight activities associated with CTC trials.
The position involves liaison with all staff at the CTC and with a wide range of academic, managerial and administrative staff in other departments within UCL, and with clinical and service staff at NHS Trusts and other trial sites.
Contact with regulatory bodies and research ethics committees regarding QA, auditing, trial oversight and monitoring issues may also be required.
The post involves line management of Quality Assurance Officer(s) and some of the Clinical Trial Moni tors.
This post is funded for two years in the first instance.
About you
The post holder will have a relevant undergraduate degree or equivalent professional experience along with considerable experience in the conduct of UK clinical trials involving Investigational Medicinal Products and an excellent understanding of relevant current clinical trial and research regulations (in particular the Medicines for Human Use (Clinical Trials) Regulations and UK Framework for Health and Social Care Research) and associated guidance documents.
Knowledge of cancer and cancer therapies and experience of hosting audits and/or GCP inspections is desirable.
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