Clinical Research Associate - Czech Republic

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 a Clinical Research Associate, you will be dedicated to one of our global pharmaceutical clients; a client with which 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.
Position overview:
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 Czech 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