Site Monitor / Clinical Research Associate I / II - FSP

When our values align, there's no limit to what we can achieve.

• 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

LI-LO1