BrightOwl Loader Loading

Clinical Research Associate France,  

Prahs (company)


Posted on : 09 October 2019

Project Description

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.


Passionate, innovative and committed.  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.
  • You will be educated to degree level in a life science discipline or be a licensed healthcare professional.
 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
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.  As a Clinical Research Associate, you will be dedicated to one of our global pharmaceutical client with whom PRA shares a culture of innovation, flexibility and a common vision of bringing life-improving drugs to market. Leading by example, you can set the standard of excellence and enjoy a challenging career in this exclusive program.  The Clinical Research Associate is ultimately responsible for the successful management of investigator sites and monitoring activities for assigned clinical studies 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, in accordance with the clinical monitoring plan.
 
  • Developing effective relationships with investigator site staff to ensure that key clinical metrics are met.
 
  • Ensuring integrity of clinical data through an ability to sufficiently maintain site tracking records and working diligently to relevant guidelines.

Locations

France

Find a Job Find Candidates

Similar Jobs

More jobs from Prahs

Other jobs in France

Other similar job in this location (country / city)

Other Jobs

Most Recent Searches

Most Famous Searches

You might also like