Clinical Research Associate

6 dagen geleden


Utrecht, Utrecht, Nederland PRA Voltijd
About the Role

We are seeking a highly skilled and detail-oriented Clinical Research Associate to join our team at ICON plc. As a key member of our operational team, you will be responsible for ensuring the development, validation, and use of analytical methods in our bioanalytical or clinical laboratory.

Your daily tasks will involve maintenance of equipment, calibration, processing samples, and injecting on instruments. You will also be part of a team responsible for quality control within the laboratory processes and supporting the reporting of data from studies.

Key Responsibilities
  • Primary processing of clinical safety samples
  • Primary processing of PK samples
  • Shipment of samples
  • Analysis of PCR, drug tests, and specific protocol-related tests
  • Monitoring of alarm systems for sample storage
  • Working with LIMS
  • Routine sample processing with different techniques
  • Interpreting and data processing/reporting results and approving or rejecting sample analysis
  • Identifying deviations and performing investigations under supervision
  • Performing peer data review for quality control
  • Ensuring compliance with GxP and other relevant regulations
What We Offer

At ICON, we are committed to developing our employees in a continuous learning culture. Our focus is to provide a comprehensive and competitive total reward package that comprises base pay, variable pay, and recognition programs. We also offer best-in-class employee benefits, supportive policies, and wellbeing initiatives to support you and your family at all stages of your career.

We are an equal opportunity and inclusive employer, 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.


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