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2017-43820

2017-43820

Title 
Dedicated Clinical Research Associate (CRA), Paris area, France
Job Locations 
-
France
Posted Date 
11/15/2017

More information about this job

Overview

At PRA Health Sciences, providing innovative solutions for our clients is what we do. Side by side with our clients, we strive to move drug discovery forward, helping them to develop life-saving and life-improving drugs. With our unique blend of expertise, we provide comprehensive clinical development services across all phases. From full service clinical development to the pioneering Embedded Solutions™ model, PRA provides a broad spectrum of solutions that meet the demands of a diverse marketplace.

As a top five CRO, we have worked on 100+ marketed drugs across several therapeutic areas and conducted the pivotal or supportive trials that led to FDA and/or international regulatory approval of 70+ such drugs.

Responsibilities

Within our Embedded Solutions model, we have exciting opportunities for Clinical Research Associates (CRAs) to be 100% dedicated to one key sponsor.

You will be a fully integrated member of the sponsor company’s research and development team.  These openings are located in Paris area.

 

Your involvement begins at site feasibility stage, with responsibility for the successful management of the site right through to close-out.

In addition to planning and conducting various site visits (feasibility, site selection, interim and close-out) in accordance with the clinical monitoring plan, you foster effective relationships with investigator site staff to ensure that key clinical metrics are met. This involves establishing innovative ways of increasing site and patient recruitment. When issues do occur, you proactively and promptly implements corrective action plans, and, when applicable, escalates issues to more senior members of the study team.

You may also design and deliver training to site staff, when appropriate.

Qualifications

The successful candidates will be able to demonstrate prior experience of working in investigator site management, including conducting monitoring visits, from either a pharmaceutical company, a CRO or a Clinical Research Institute/Unit. Fluency in French and English is essential.

 

Join us and you will play a fundamental role in our client’s drug development process. You will be offered a permanent contract as well as future opportunities for growth and development within our organization. Together with a competitive salary, we offer a comprehensive range of benefits and an excellent working environment.

 

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

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