PRAHS

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2017-44297

2017-44297

Title 
Clinical Trial Coordinator
Job Locations 
-
United Kingdom-Reading
Posted Date 
12/21/2017

More information about this job

Overview

At PRA, we don’t make our 15000+ people great. It’s the other way around. As we have grown to a top-5 CRO, we have maintained the feel of a small company, dedicated to collaboration and passion for what we do. We always have a desire to keep seeking new and better ways to operate. We don’t settle for the same old ways. Our passion for improving patient lives worldwide permeates all that we do. Put simply, we care.

 

As an outsourced Clinical Trial Coordinator (CTC) you will be dedicated to one of our global pharmaceutical clients; a prestigious organization, specialising in a niche rare disease, complemented by a pipeline in other therapeutic areas, including oncology. A company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program.

 

Responsibilities

The Clinical Trials Coordinator is responsible for providing daily support to the Clinical Project Managers in all aspects of clinical trial activities. He/She will perform routine duties associated with document management and submission to the Trial Master File, as well as assisting with the activities of the study team and associated vendors. The
Clinical Trials Coordinator works under direct supervision on tasks that require minimal discretion.

 

The CTC prepares and revises documents such as protocols, informed consent forms and guidelines, and routes documentation for appropriate signage.Communicates with CROs on behalf of Clinical Project Managers to ensure the efficient conduct of clinical trials. Assists with ordering of materials needed for clinical studies. Collects, organizes and prepares regulatory documentation for transfer to Trial Master File and assists with tracking of documents under guidance. Performs various other duties as assigned. 

 

Qualifications

You are:

 

Detail-orientated, passionate and reliable. Here at PRA we want our employees to succeed and ensure that they are set up for this success through constant training, development and support. To enable success in this position you will have:

 

  • 2 years’ experience in clinical project administration or other relevant experience
  • Associate’s degree or international equivalent in business, finance, health sciences or related field is preferred but not essential.


Your health, your family, your career, your money — the things that matter to you, matter to us. The benefits of PRA just get better and better. PRA Health Sciences is an Equal Opportunity Employer. We welcome and encourage diversity in the workplace. For more information please visit our website: www.prahs.com

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