PRAHS

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2017-44015

2017-44015

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

More information about this job

Overview

PRA Health Sciences is an award winning CRO.

 

We are proud to have won Pharma Times 'Clinical Research Company of the Year' in 2017 for the fourth consecutive year. We aren’t winning these awards by chance; PRA is being recognised industry-wide for our dedication to the future of clinical development. Most importantly for you, at PRA we recognise that our success is down to our people.

Responsibilities

 

Working as an integral part of the PRA full-service study team and for a varied mix of sponsors, 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 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.

Qualifications

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:

 

  • 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 dPRA Health Sciences is an Equal Opportunity Employer. We welcome and encourage diversity in the workplace.egree level, have equivalent experience 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.

 

 

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