Clinical Trial Assistant

1 week ago


Uxbridge, United Kingdom Parexel Full time

When our values align, there's no limit to what we can achieve.

Parexel are currently recruiting for an experienced Clinical Trial Assistant to support one of our key sponsors, and one of the most renowned pharmaceutical businesses in the world.

In this position you will be an invaluable team member collaborating with the wider global study team whilst being responsible for multiple tasks that span from study start up to study close out which enables the efficient execution of clinical trials to high quality standards

Some specifics about this advertised role

Responsible for providing study level operational support to the study team from study start up to close out and submission. Maintains and oversees of study team shared spaces. Trial Master File (TMF) maintenance, compliance, and oversight Analyse, interpret, and follow up on metrics. Maintains and oversees Study Team on Demand (STOD)Update all appropriate Clinical Trial Management Systems (CTMS) on an ongoing basis, including performing regular reviews of site level data in clinical systems. Ensure timely and high quality data entry compliance from sites, manage and submit all relevant documents to the TMF, ensuring first time quality.

Who are Parexel

Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base.

We supported the trials of most of today's top 50 best-selling drugs, but equally we enable more niche drug developments that are critical to the well-being of many patients.

You'll be an influential member of the wider team.

What we are looking for in the this role

For every role, we look for professionals who have the determination and courage always to put patient well-being first.

That to us is working with heart.

Here are a few requirements specific to this advertised role.

Scientific related degree is essential. Relevant clinical research or clinical trial experience, ideally gained within complex global studies. Experienced with clinical trial processes and applicable systems. Knowledge of drug development process. Fluent in English.

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