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Clinical Research Associate
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Clinical Research Associate
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Uxbridge, United Kingdom Parexel Full timeParexel's MissionWe are in the business of improving the world's health by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments.Role OverviewThis Clinical Research Associate role offers the opportunity to go beyond the role of a typical clinical monitor. As the clinical sites'...
Clinical Research Associate
2 months ago
About the Role
Parexel is seeking a skilled Clinical Research Associate to join our Clinical Operations Team in the UK. As a key member of our team, you will be responsible for building and maintaining site relationships, ensuring site quality and delivery, and managing site integrity.
Key Responsibilities
- Conduct qualification visits, site initiation visits, monitoring visits, and termination visits at assigned clinical sites.
- Build relationships with site staff and ensure the integrity of the study.
- Protect patients by reviewing the performance of the trial at designated sites and ensuring compliance with protocol and regulatory requirements.
- 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.
- Monitor the completeness and quality of regulatory documentation and perform site document verification.
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.
- 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.
About Parexel
Parexel is a leading biopharmaceutical services company that helps clients transform scientific discoveries into new treatments. We believe in our values of Patients First, Quality, Respect, Empowerment, and Accountability, and we are committed to improving the world's health.
