Clinical Trial Monitor

1 month ago


Québec, Quebec, Canada Parexel Full time
Job Description

Parexel Clinical Trial Monitor

Parexel is seeking a highly skilled Clinical Trial Monitor to join our team. As a Clinical Trial Monitor, you will be responsible for ensuring the smooth conduct of clinical trials at investigator sites.

Key Responsibilities
  • Ensure regulatory compliance with ICH-GCP and local regulations
  • Conduct site visits and monitoring activities to ensure data integrity and subject safety
  • Verify informed consent and ensure confidentiality of subject data
  • Manage site-level activities and communication to ensure project objectives are met
  • Collaborate with site staff and other stakeholders to resolve issues and ensure audit readiness
  • Provide guidance on Good Clinical Practice and regulatory requirements
Requirements
  • Bachelor's degree or RN in a related field or equivalent combination of education, training, and experience
  • Minimum 1 year experience as a clinical monitor with demonstrated experience of monitoring (virtual or onsite)
  • Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements
  • Excellent communication, presentation, and interpersonal skills
  • Ability to manage required travel of up to 75% on a regular basis
Preferred Qualifications
  • Demonstrated experience of utilizing systems like Siebel CTMS, eTMF, eISF (Florence)
  • Proficiency in local language preferred. English is required

About Parexel

Parexel is a leading global biopharmaceutical services company. We provide a comprehensive range of services to help our clients succeed in the development and delivery of innovative new treatments.



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