Senior Clinical Research Associate

3 weeks ago


Uxbridge, United Kingdom Parexel Full time
Join Our Team as a Senior Clinical Research Associate

About the Role

Parexel is seeking a highly skilled Senior Clinical Research Associate to support our UK operations. As a key member of our team, you will be responsible for site management and monitoring activities across assigned oncology studies.

Key Responsibilities

  • Manage and monitor clinical trials sites to ensure compliance with regulatory requirements and study protocols.
  • Work closely with industry leaders and subject matter experts to ensure high-quality trial execution.
  • Mentor junior CRAs to develop their skills and expertise.
  • Utilize world-class technology to streamline trial management and monitoring.
  • Contribute to the drug development process by providing critical insights and recommendations.

Requirements

  • Substantial site management experience with a strong understanding of clinical trial methodology and terminology.
  • Experience in monitoring oncology clinical trials, with a willingness to learn and adapt.
  • Effective time management, organizational, and interpersonal skills, with the ability to multi-task and prioritize.
  • Good understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH, and country clinical research law and guidelines.

What We Offer

Parexel offers a dynamic and supportive work environment, with opportunities for professional growth and development. As a Senior Clinical Research Associate, you will have the chance to work on exciting projects, collaborate with industry leaders, and contribute to the development of life-changing treatments.



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