Clinical Research Associate: ‑Site Monitor
Listed on 2026-10-12
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Research/Development
Research Assistant/Associate, Clinical Research
IQVIA is seeking a Clinical Research Associate to perform monitoring and site management to ensure sites conduct studies and report data per protocol, regulations, and sponsor requirements.
Responsibilities include site visits, recruitment tracking, training, communication with sites, and escalation of quality issues; manage regulatory submissions, CRF, data queries; ensure TMF/ISF documentation. The role requires 1 year of on-site CRA experience and a science/healthcare background.
This role is for the Clinical Research Associate:
On‑Site Monitor role at IQVIA Argentina.
The advertised compensation is 72..
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:
On‑Site Monitor role in the description above.
We appreciate your interest in this position.
Join IQVIA Argentina and contribute to our ongoing work.
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