PRA Health Sciences

Senior Clinical Research Associate - Oncology Experienced

Location
Czech Republic, Prague, Home based
Salary
Competitive
Posted
23 Feb 2021
Closes
25 Mar 2021
Ref
SG2020-70131
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Commitment to our staff is only surpassed by our commitment to advancing treatment options available to patients. We understand the importance of supporting and investing in our people. With 20% of our employees promoted last year, we don’t need to tell you that your career will thrive at PRA. We know it. And we can prove it. As we grow, so will you. Come discover your PRA.

Working fully embedded within one of our pharmaceutical clients, with the support of PRA right behind you, you’ll be at the heart of our client’s innovation.

As a Senior Clinical Research Associate, you will be dedicated to a one of our global Biotechnology clients who have an emerging presence in Europe and who are committed to improving lives of patients though innovative and transformative therapies.

The Clinical Research Associate is ultimately responsible for the successful management of investigator sites and monitoring activities for assigned clinical studies 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, in accordance with the clinical monitoring plan.
  • Developing effective relationships with investigator site staff to ensure that key clinical metrics are met.
  • Ensuring integrity of clinical data through an ability to sufficiently maintain site tracking records and working diligently to relevant guidelines.

Passionate, innovative and committed.

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 degree level in a life science discipline or be a licensed healthcare professional.
  • Experience working on Oncology trials or complex studies would be an advantage for this role.
  • Fluency in English and Czech is required.

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.


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