Clinical Trial Monitor

at  Imperial College London

Hammersmith, England, United Kingdom -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate10 Feb, 2025GBP 55240 Annual10 Nov, 2024N/AGood communication skillsNoNo
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Description:

AVAILABLE DOCUMENTS

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

  • Download: Job Description Clinical Trial Monitor MED04933.Pdf
  • Download: Employee Benefits Booklet.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.

Responsibilities:

ABOUT THE ROLE

We are looking for a successful and dynamic Clinical Trial Monitor/Manager to assist with running three multi-centre clinical trials, led by Professor Sudhin Thayyil in the Centre for Perinatal Neuroscience. The trials have a focus on hypoxic ischemic encephalopathy, a birth related brain injury which impacts around three million babies every year, predominantly in low and middle-income countries. The trials are:

  • PREVENT (Prevention of Epilepsy by reducing Neonatal Encephalopathy) study involving 60,000 women from several hospitals in India (NIHR RIGHT program). This is the world’s largest study on babies with birth related brain injury.
  • EMBRACE trial (Erythropoietin Monotherapy in Neonatal Encephalopathy in Low- and Middle-income countries) in India and Bangladesh involving 500 babies from several hospitals in India and Bangladesh (Thrasher foundation).
  • COMET (Cooling in Mild Encephalopathy) trial involving 430 babies with mild encephalopathy from 40 NHS hospitals funded by NIHR HTA program.

WHAT YOU WOULD BE DOING

As the Clinical Trial Monitor/Manager, you would be working primarily on the PREVENT and EMBRACE studies. You will assist with the management and monitoring of the trials and helping with data analysis and publication preparation. This will include building partnerships with oversea stakeholders, ensuring ethical approvals are maintained, and leading on development and delivery of the monitoring plan. You will work closely with the COMET trial’s Clinical Trial Manager and the EMBRACE study’s Clinical Project Manager, to ensure coordinated submission of regulatory and financial reporting.


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Proficient

1

Hammersmith, United Kingdom