Clinical Trial Monitor

Campus: Hammersmith / Stadium House 

We are seeking to appoint a Clinical Trial Manager within the Imperial Prostate team led by Professor Hashim Ahmed; a group that has an international reputation in this field with regular visitors from Europe and North America to learn research and clinical techniques proposing a change in the prostate cancer diagnosis and therapeutic pathway. We have a portfolio of numerous clinical trials that are either completed or ongoing. 

This post will be based within the Department of Surgery and Cancer, both in Imperial Prostate at Hammersmith Hospital led by Professor Hashim Ahmed and the UKCRC registered Imperial Clinical Trials Unit (ICTU). 

Duties and responsibilities

• You will oversee a PCUK and NIHR funded clinical trial called TRANSFORM in screening of prostate cancer and will be responsible for all aspects of trial monitoring including close liaison with the Chief Investigator, PIs and teams at other centres, by implementing/adapting established ICTU systems to ensure the trial is conducted to the highest scientific and regulatory standards
• At the commencement of the study, you will also be responsible for assisting the Trial Manager and the Project Manager and wider team in all aspects of setting up of the study
• To ensure that the studies are conducted in compliance with protocol, overall clinical objectives, ICH GCP and the ICTU SOPs and are run according to agreed timelines
• To train the staff from the research sites in the conduct of the study, documentation, record keeping and regulations
• To maintain central records for the research sites including maintenance of the Trial Master Files (TMFs) as well as creation and distribution to sites of the Investigator Site Files (ISFs)
• To set up and attend regular meetings with study staff, with staff at the co-ordinating centres, and to facilitate communication between them 

Essential Requirements

• A science degree (BSc) or equivalent vocational qualification, or equivalent experience
• Previous clinical trials experience
• Previous monitoring experience
• Knowledge of Good Clinical Practice (GCP) and relevant regulations
• Evidence of strong IT literacy (MS Office)
• Experience of data management processes using electronic CRFs
• Experience of working within the NHS or academic clinical research setting
• Experience in monitoring prostate and/or cancer trials

Further Information

This post is full-time, fixed-term for 12 months in the first instance and you will be based at Hammersmith Campus.

Should you require any further details on the role please contact: Olivia Barrett – olivia.barrett@imperial.ac.uk.

Closing date: 26 June 2024

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