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Clinical Research Associate II/Senior

  1. Sofia
JR113033
  1. Clinical Monitoring
  2. ICON Full Service & Corporate Support
  3. Remote

About the role

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Join ICON plc in Bulgaria as a Clinical Research Associate (CRA)

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.

Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.

That’s our vision. We’re driven by it. And we need talented people who share it.
If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.

Role Overview: As a Clinical Research Associate (CRA) at ICON plc, you’ll play a pivotal role in the execution and management of clinical trials. You will ensure the integrity of the studies, adherence to protocols, and compliance with regulatory standards.

Key responsibilities:

  • Conduct site evaluation, initiation, monitoring and close-out visits
  • Ensure compliance with the study protocol, regulatory requirements and company procedures
  • Build and maintain strong relationships with investigators, site staff, and study teams
  • Perform site management activities to ensure the quality and integrity of the studies
  • Monitor and report study progress, handling and resolving site issues

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: ICON offers a dynamic and rewarding work environment where your contributions make a real difference. You’ll have the opportunity to grow and develop in your career within a global organization dedicated to advancing healthcare.

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.

ICON 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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