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CRA II / Senior CRA

Employer
ICON Plc
Location
Poland, Homeworking
Salary
Competitive
Start date
9 Jun 2024
Closing date
9 Jul 2024

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Job Details

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.

CRA II / Senior CRA

Location: Warsaw Poland (office or home based anywhere in Poland)

Role overview: Embrace the challenge as a Clinical Research Associate (CRA) at ICON plc in Poland, 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 in ICON:

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.

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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