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Job Details

CLINICAL RESEARCH ASSOCIATE (CRA) - Slovakia

Company: PRA Health Sciences
Location: Slovakia
Reference: MH-2018-44518
Closing Date: 15 Mar 18
Type: Full Time
Salary (£): Competitive
Benefits: Excellent Salary and Benefits

Job Summary:

An outstanding opportunity to join one of the world’s leading contract research organisations and be part of a dynamic and growing international company. Join PRA Health Sciences as a Clinical Research Associate (CRA) and help realize your career potential.

Requirements:

CLINICAL RESEARCH ASSOCIATE (CRA)

Location: Slovakia

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. Enter: the Strategic Solutions Division.

As Clinical Research Associate, you will be dedicated to one of our global pharmaceutical clients; a science-based company with one of the most exciting product pipelines in the industry. This global pharmaceutical client develops breakthrough innovative medicines to improve and extend people’s lives in oncology, general medicine and eye care. Working in this way, you will have the opportunity to build your career in a rewarding customer-focused environment that supports creativity, collaboration and performance.

Responsibilities:

We are seeking an experienced Clinical Research Associate to work as an integral part of our pharma client’s global study team. 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

You will receive the support you need to develop personally and professionally and work in an environment where you matter. 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.

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, have equivalent experience or be a licensed healthcare professional.
  • Fluency in written and spoken Slovak and English.

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.

If you have any questions please email recruiteruk@prahs.com or call our recruitment department at +44 (0) 1189 213 652

For more information please visit our website: www.prahs.com

Apply for this job: CLINICAL RESEARCH ASSOCIATE (CRA) - Slovakia

Contact Information:

Address:  Head Office
500 South Oak Way
Green Park
Reading
Berkshire
RG2 6AD
England
Tel:  +44 (118) 918 1000
Fax:  +44 (118) 918 1001
Website:  Visit Our Web Site

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