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SCRA

  1. Prague
JR118157
  1. Clinical Monitoring
  2. ICON Full Service & Corporate Support

About the role

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Join the innovation wave – ICON plc seeks dynamic Clinical Research Associate(CRA) in the Czech Republic

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.

With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.

Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

Role overview: Embrace the challenge as a Clinical Research Associate (CRA) at ICON plc in CZE, where you'll be at the forefront of transformative clinical trials. Your role will be pivotal in upholding the integrity of studies, ensuring adherence to protocols, and navigating complex regulatory landscapes.

Key Responsibilities:

  • Navigate uncharted territories through site evaluations, initiation, monitoring, and close-out visits
  • Champion compliance with study protocols, regulatory standards, and company procedures
  • Foster invaluable connections with investigators, site staff and study teams
  • Steer the ship in site management activities to safeguard the quality and integrity of the studies
  • Illuminate the path forward by monitoring and reporting study progress while proactively troubleshooting site issues
  • Potential assist in training and mentoring fellow CRAs

Qualifications:

  • 18+ months of monitoring experience in phase I-III trials as a CRA
  • College degree in medicine, science or equivalent
  • Previous monitoring experience in medium-sized studies, including study start-up and close out
  • Good knowledge of ICH-GCP guidelines, local regulatory standards and clinical trial processes
  • Strong communication, organizational, and problem-solving skills
  • Ability to travel and work independently
  • Availability to travel least 60% of the time (international and domestic – fly and drive) and should posses a valid driving license

Benefits working at ICON: At ICON, innovation isn’t a buzzword; it’s a way of life. Be part of a dynamic and rewarding environment that actively shapes the future of healthcare. Grow and thrive in your career within a global organization committed to enhancing the quality of life for people worldwide.

Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.

At ICON, our focus is to provide you with a comprehensive and competitive total reward  package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs.  In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career – both now, and into the future. stages of your career - both now, and into the future.  

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

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