Clinical Research Associate

4 weeks ago

Uxbridge, United Kingdom Parexel Full time

Parexel's Mission

Parexel is a leading biopharmaceutical services company dedicated to improving the world's health. We achieve this by providing a comprehensive suite of services that help our clients transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our expertise is underpinned by a deep conviction in our values: Patients First, Quality, Respect, Empowerment & Accountability.

About the Role

We are currently seeking a Clinical Research Associate to join our Clinical Operations Team in the UK. This role offers the opportunity to go beyond the typical clinical monitor and work closely with clinical sites to ensure their success. As the sole point of contact, you will be responsible for addressing and resolving site issues and questions, managing site quality and delivery, and promoting the development of life-changing treatments for patients.

Key Responsibilities

  • Leverage your expertise to conduct qualification visits, site initiation visits, monitoring visits, and termination visits at assigned clinical sites, generating visit/contact reports.
  • Build relationships with clinical sites, promoting rapport and utilizing problem-solving skills to ensure the integrity of the study.
  • Protect patients by reviewing the performance of the trial at designated sites, ensuring the rights and well-being of human subjects are safeguarded and in accordance with protocol.
  • Drive productivity by developing patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines, ensuring compliance with approved standard operating procedures, protocol/amendments, GCP, and applicable regulatory requirements.
  • Ensure quality by evaluating the quality and integrity of reported data, site efficacy, and drug accountability.
  • Execute monitoring activities, including site document verification and regulatory documentation.

Requirements

  • Site Management or equivalent experience in clinical research, with 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.
  • Experience working in a self-driven capacity, with a sense of urgency and limited oversight.
  • Client-focused approach to work and flexible attitude with respect to assignments/new learning.
  • Ability to manage multiple tasks, evaluate unpredictable scenarios, and achieve project timelines while applying understanding of study protocol(s).
  • Honest and ethical work approach to promote the development of life-changing treatments for patients.
  • Strong computer skills, including knowledge of 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, catered to your individual experience. You can anticipate less travel and a lower protocol load compared to industry peers. Our bonus incentive program, opportunities to work within multiple therapeutic areas, and career advancement opportunities make us an attractive choice for those seeking a rewarding career in clinical research.

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