Everything we do has the potential to impact patient lives, and our Clinical Research Associates (CRAs) take their work seriously, demonstrate empathy, and act with heart. They also perform with urgency, navigating our streamlined clinical operating model to drive effectiveness, reduce handoffs and increase employee, client and site satisfaction.
As a CRA at Parexel, you‘ll be joining a team with a wide variety of experiences and knowledge. We’re looking for people like you to take the initiative to do things better and smarter—people who want to grow personally and professionally. We recognize and uphold the importance of all people, the way we do things, our quest for innovation, and most importantly, our patients.
- Full Time
- Level: Mid
- Travel: Yes
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Success Profile
Check out the top traits we’re looking for and see if you have the right mix.
- Innovative
- Problem-Solver
- Communicator
- Tech-Savvy
- Confident
- Independent
Rewards
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Global Impact
We are one truly global team working together to propel each client´s journey ahead faster.
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Balance
We value work-life balance. We try and keep regular hours and an emphasis on life outside the office.
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Collaboration
Work with industry leaders and subject matter experts.
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Freedom
The ability to innovate, ask “what if” and try new solutions without fear of failure.
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Variety
Opportunities to work on multiple accounts – never boring!
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Compensation
Competitive salaries and bonus structure based on individual metrics.
Responsibilities
***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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