Clinical Trial Assistant

at  Imperial College London

WHAT WE ARE LOOKING FOR

We are seeking to appoint a hardworking, enthusiastic and dynamic individual who is keen to develop their experience in all aspects of clinical research delivery. You must hold A-Levels or equivalent experience. A flexible attitude is essential as you will be working on multiple projects simultaneously within the role.

Desirable experience includes:

• Experience working in a patient-facing role.
• Experience working in clinical research delivery/administration
• Working knowledge of the current EU Clinical Trials Directive, UK Clinical Trials regulations, Principles of GCP, General Data Protection Regulation (GDPR) and Research Governance Framework legislation.

AVAILABLE DOCUMENTS

Attached documents are available under links. Clicking a document link will initialize its download.

• Download: Employee Benefits Booklet.Pdf
• Download: Job Description Clinical Trial Assistant.Pdf

Please note that job descriptions are not exhaustive, and you may be asked to take on additional duties that align with the key responsibilities mentioned above.
We reserve the right to close the advert prior to the closing date stated should we receive a high volume of applications. It is therefore advisable that you submit your application as early as possible to avoid disappointment.
If you encounter any technical issues while applying online, please don’t hesitate to email us at support.jobs@imperial.ac.uk. We’re here to help.

ABOUT THE ROLE

We have an exciting opportunity for a Clinical Trial Assistant role that will work alongside the Imperial College Healthcare NHS Trust (ICHNT) Clinical Research Delivery Teams and supported by Imperial College London’s Cancer and Haematology Academic Research Team. The Cancer & Haematology Academic Research Team are a research support unit working across both Imperial College London and Imperial College Healthcare NHS Trust and other affiliated NHS Trusts, delivering clinical trials of all phases.
This is a fantastic opportunity for somebody looking for a comprehensive introduction to the oncology clinical research industry.

WHAT YOU WOULD BE DOING

You will primarily oversee the coordination and delivery of a cancer surveillance research study, in close collaboration with the ICHNT Hepatology team as well as the Chief and Principal Investigator. In addition, you will support the ICHNT Oncology Research Delivery teams with a portfolio of other hepatocellular carcinoma (HCC) and neuroendocrine tumour (NET) Phase I-III clinical trials. This support will include ensuring high-quality and accurate research data is collected and entered onto electronic case report forms (eCRFs) maintaining up-to-date Investigator Site Files (ISFs) and ensuring the trials are conducted to the highest scientific, ethical and regulatory standards.