Clinical Research Associate

1 week ago


Québec, Quebec, Canada Parexel Full time
About the Role

Parexel is seeking a highly skilled Clinical Research Associate to join our team. As a CRA, you will be responsible for building and maintaining strong relationships with clinical sites, ensuring their success and quality delivery.

Key Responsibilities
  • Conduct qualification visits, site initiation visits, monitoring visits, and termination visits at assigned clinical sites, generating visit/contact reports.
  • Develop and maintain relationships with site staff, promoting rapport and ensuring the integrity of the study.
  • Review site performance, ensuring the rights and well-being of human subjects are safeguarded and in accordance with protocol.
  • Develop patient recruitment strategies with clinical sites to meet enrollment timelines, ensuring compliance with SOPs, protocol, GCP, and regulatory requirements.
  • Evaluate the quality and integrity of reported data, site efficacy, and drug accountability.
  • Monitor completeness and quality of Regulatory Documentation and perform site document verification.
About Us

Parexel is a leading Clinical Research Organization with a global presence. Our team members are passionate about delivering high-quality results and making a meaningful impact in the lives of patients. We offer a collaborative and supportive work environment, with opportunities for career growth and development.

Requirements
  • 18+ months of direct onsite monitoring experience as a Clinical Research Associate (CRA)
  • 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
  • Ability to work in a self-driven capacity with a sense of urgency and limited need for oversight
  • Client-focused approach with a flexible attitude towards assignments and 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 CTMS, EDMS, and MS-Office products
  • Fluency in both English and French


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