Clinical Research Associate: Site Monitoring & Coordination
Listed on 2026-10-15
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Research/Development
Research Assistant/Associate, Clinical Research -
Healthcare
Clinical Research
IQVIA is seeking a Clinical Research Associate to monitor sites and ensure adherence to the study protocol, regulatory requirements, and sponsor expectations. You will conduct site visits, administer training, and manage communications with site personnel.
The role requires prior on-site monitoring experience, strong regulatory knowledge, and excellent English communication. Proficiency with EDC/CTMS/eTMF is preferred, with potential travel to sites as needed.
The following position is for a Clinical Research Associate:
Site Monitoring & Coordination with IQVIA.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Clinical Research Associate:
Site Monitoring & Coordination role in the description above.
We appreciate your interest in this position.
Join IQVIA and contribute to our ongoing work.
Take a moment to read everything above and see whether this role is right for you.
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