PRAHS

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2017-43970

2017-43970

Title 
Clinical Project Assistant - Office Based, Laval (Canada)
Job Locations 
-
Canada-QC
Posted Date 
12/8/2017

More information about this job

Overview

Do you want to watch clinical development change, or do you want to be the one to shape it?

 

Because we’re hoping you’re here for the latter.

Responsibilities

Who are we?

We Are PRA.

 

We are 15,000 employees strong, operating in more than 85 countries. We are committed to saving lives, and we are constantly striving to be the best at what we do. Our impact is real and we see it every single day. We are getting live saving drugs into the hands those who need them most.

 

Who Are You?

You are an experienced Clinical Project Assistant who is responsible for operational support of Clinical Studies. You can provide excellent support to not only your project teams but also to clients. You are excited and enthusiastic. Most of all, you want to do it in a place where you’re more than an employee number. A place you love working.

 

Still here? Good. Because if this is you, we’d really like to meet you.

 

What will you be doing?

As a Clinical Project Assistant, you will be responsible for supporting clinical trials in North America, across a variety of therapeutic areas. You will have a wide range of responsibilities. We’re including a few of the big ones.

  • Coordinate with the clinical project team the distribution, retrieval and review of regulatory documents required for initiation of a clinical trial.
  • Assure the accuracy of required clinical trial documents maintained within LSF throughout the clinical trial.
  • Generate grant payments requests, maintains tracking tool for each study and resolves payment inquiries from investigator sites.
  • Prepare necessary study supplies for clinical trials and processes site requests for shipping supplies, as needed.
  • Maintenance of clinical trial tracking systems.

Qualifications

What do you need to have?

  • 0 – 2 years of related experience
  • Prior experience using computerized information systems
  • Read, write, and speak fluent English & French; fluent in host country language required
  • undergraduate degree or relevant industry experience required
  • Clinical trials support or pharmaceutical industry experience preferred
  • Experience with PC-Windows, word processing, and electronic spreadsheets preferred
  • Office based or clinical employment experience preferred
  • Knowledge of ICH and local regulatory authority drug research and development regulations preferred

PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.

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