Sr Clinical Research AssociateSite Monitor II - FSP
Sr Clinical Research AssociateSite Monitor II - FSP
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1 Vacancy
Job Description
When our values align theres no limit to what we can achieve.
At Parexel we all share the same goal to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special a deep conviction in what we do.
Each of us no matter what we do at Parexel contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally we do it with empathy and were committed to making a difference.
***Qualified candidates must be fluent in French***
PAREXEL FSP is currently looking for Site Monitors to join our expanding team. Working as a Site Monitor at Parexel FSP offers longterm 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 onsite 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 followup actions.
Experience required for this role:
For every role we look for professionals who have the determination and courage always to put patient wellbeing first. That to us is working with heart.
The Site Monitor should have at least 3 years ofdemonstrated experience of monitoring and will need to speak the local language of the countries they will monitor in
Bachelors 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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Required Experience:
Senior IC
Employment Type
Full Time
