Clinical Research Associate/Site Monitor I/II - FSP
Canada, Remote Additional Locations Remote,Canada Job ID R0000032193 Category Clinical Trials Date Posted 03/19/2025Overview
As a Clinical Research Associate (CRA) at Parexel, you act as an integral part to get treatments to patients sooner. Our CRAs' priority is the safety and well-being of the patients. As you travel to investigator sites and perform your monitoring duties, we encourage you to be inquisitive, take accountability, build relationships, and act with integrity.
Join a team with a wide variety of experiences and knowledge, and work on global projects within a broad scope of therapeutic areas. We’re looking for people who want to grow personally and professionally and support their colleagues globally and cross-functionally.
Success Profile
Do you have these soft skills and interpersonal traits to succeed at Parexel?
- Communicator
- Detail-oriented
- Flexible
- Organized
- Problem-solver
- Self-starter
About This Role
***Bilingual in French highly preferred***
PAREXEL FSP is currently looking for Site Monitors to join our expanding team.Working as a Site Monitor at Parexel FSP offers long-term job security and excellent career prospects. Parexel FSP supports clinical studies across a full range of therapeutic areas, and we have longstanding partnerships with a vast client base.
Role Summary:
You will be responsible for data integrity, data quality and ensuring compliance with ICH GCP and local requirements at the site level.
Monitoring will be conducted in line with the Study Monitoring Plan and will be performed virtually for most activities to supplement on-site visit requirements.
The Site Monitor will collaborate with the Site Manager to assure that the site is in compliance with the protocol and is inspection ready.
You will provide guidance at the site and project level towards audit readiness standards and supports preparation for audit and required follow-up actions.
Experience required for this role:
For every role, we look for professionals who have the determination and courage always to put patient well-being first. That to us is working with heart.
The Site Monitor should have at least 1 year of demonstrated experience of monitoring and will need to speak the local language of the countries they will monitor in
Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience
Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements
Ability to adapt to changing technologies and processes
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Potential Career Path
Parexel offers various career paths and internal development programs for CRAs to advance to the next level. This could include enhancing your technical position, moving into management, or shifting to other areas of the business.
- APEX CRA
- CRA I
- CRA II
- Senior CRA
- Project ManagementSubject Matter ExpertPeople Management
Employee Insights
TEAM IMPRESSIONS
Why Clinical Research Associates work at Parexel
