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Clinical Research Associate – PRA Health Sciences

Offre publiée le lundi 30 novembre 2020

One thing we all have in common is the drive to produce great results for our clients and to advance treatment options available to patients worldwide. We always have a desire to keep seeking new and better ways to operate, to achieve these results.

Leveraging the advantages of working for a top-5 CRO, whilst simultaneously working fully-dedicated to a leading pharma company, will guarantee that the results you help accomplish in drug development are matched by your own career achievements.

We are looking for a CRA based in France to work dedicated to one of our sponsors.

As a Clinical Research Associate, you will be dedicated to one of our global pharmaceutical clients, a company that values performance, recognizes merit and has a high focus on quality. This environment encourages innovation, individuality and embraces people that want to be a part of it.

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 Clinical Operations 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 pushes forward together. United in solving problems, developing close site relationships and reaching the end goal. Operating as a key part of a global study team, the CRA plays a fundamental role in our clients’ drug development processes.

 

You are:

Dedicated, collaborative and inspire others.

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:

  • Recent and solid experience as a CRA (at least 1 year) 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, have equivalent experience or be a licensed healthcare professional.
  • Fluency in English and French is an absolute requirement
  • Experience in oncology studies will be an asset.

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.

You are interested in a new challenge and wish to join a dynamic CRO, we would love to speak with you.

Feel free send your application on my email address:  GhedjatiMina@prahs.com

In our Career Page, you will a broad range of exciting roles currently open at PRA Health Sciences:  https://prahs.com/careers

Offre publiée le mercredi 20 janvier 2021
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