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2017-43748

2017-43748

Title 
Clinical Research Associate
Job Locations 
-
Netherlands
Posted Date 
12/5/2017

More information about this job

Overview

Providing innovative solutions for our clients is what we do. But innovation just for the sake of innovation isn’t why we do it. Side-by-side with our clients, we strive to move drug discovery forward, to help them develop life-saving and life-improving drugs. We help change people’s lives for the better every single day. It’s who we are. And it’s who you could be too.

Working fully embedded within one of our pharmaceutical clients, with the support of PRA right behind you, you’ll be at the heart of our client’s innovation.

Responsibilities

Working fully embedded within one of our pharmaceutical clients, the Clinical Research Associate is ultimately responsible for the successful management of investigator sites throughout the trial lifecycle.

 

Key responsibilities include:

  • Full ownership of investigator sites for assigned studies with responsibility for the successful management of the site right through to close-out.
  • Planning and conducting various site visits (feasibility, site selection, interim and close-out) in accordance with the clinical monitoring plan.
  • Developing effective relationships with investigator site staff to ensure that key clinical metrics are met.
  • Preparing for and attending investigator meetings, coordinating the timely shipment and the subsequent proper storage and accountability of clinical supplies and following-up of drug safety issues.
  • Ensuring integrity of clinical data through an ability to sufficiently maintain site tracking records and work diligently to relevant guidelines.

We believe our Local Study Team is second to none. You will receive the support you need to develop personally and professionally and work in an environment where you matter. Our team help to speed the development of life-changing therapeutics and to make a distinctive contribution to the health and well-being of patients.

Qualifications

“If you have the passion to innovate, we’ll give you the power to change”

 

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:

  • Prior experience of working in investigator site management, including conducting monitoring visits, from either a pharmaceutical company or a CRO environment.
  • A working knowledge of ICH-GCP guidelines and local and international regulatory requirements is essential.
  • A degree level, have equivalent experience or be a licensed healthcare professional.
  • Fluent Dutch and English.

 

Your health, your family, your career, your money — the things that matter to you, matter to us

If you’d like more information about the specific benefits available in your country, the Talent Acquisition team will be happy to provide it.

 

 

If you’d like more information about the specific benefits available in your country, the Talent Acquisition team will be happy to provide it.

PRA Health Sciences is an Equal Opportunity Employer. We welcome and encourage diversity in the workplace.

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