Clinical Research Associate II

1 maand geleden


Amsterdam, Noord-Holland, Nederland Parexel Voltijd
Join Our Team as a Clinical Research Associate II

Parexel is a leading provider of biopharmaceutical services, and we're currently seeking a highly skilled Clinical Research Associate II to join our Clinical Operations Team in the Netherlands.

About the Role

This is an exciting opportunity to work in a dynamic and fast-paced environment, where you'll be responsible for building and maintaining relationships with clinical sites, ensuring their success, and promoting the development of life-changing treatments for patients.

Key Responsibilities
  • Conduct qualification visits, site initiation visits, monitoring visits, and termination visits at assigned clinical sites, generating visit/contact reports.
  • Build relationships with site staff, promoting rapport and ensuring the integrity of the study.
  • Protect patients' rights and well-being, reviewing the performance of the trial at designated sites.
  • Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines.
  • Evaluate the quality and integrity of reported data, site efficacy, and drug accountability.
  • Execute monitoring activities, ensuring the completeness and quality of Regulatory Documentation and performing site document verification.
Requirements

To be successful in this role, you'll need:

  • Site Management or equivalent experience in clinical research, with a strong understanding of clinical trials methodology and terminology.
  • Ability to perform all clinical monitoring activities independently.
  • Bachelor's or equivalent degree in biological science, pharmacy, or other health-related discipline.
  • Strong interpersonal, written, and verbal communication skills within a matrixed team.
  • Fluent knowledge of the Dutch and English languages.
  • Experience working in a self-driven capacity, with a sense of urgency and limited oversight.
  • A client-focused approach to work and flexible attitude with respect to assignments/new learning.
  • The ability to manage multiple tasks, evaluate unpredictable scenarios, and achieve project timelines.
  • An honest and ethical work approach to promote the development of life-changing treatments for patients.
  • Strong computer skills, including knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS), and MS-Office products such as Excel and Word.
What We Offer

Parexel offers a world-class technology and training program, a bonus incentive program, and opportunities to work within multiple therapeutic areas. If you're passionate about clinical research and want to make a meaningful impact, we encourage you to apply for this exciting opportunity.



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