Clinical Trials Lead Site Coordinator

PSI CRO · Mendoza

New

Mid 🇬🇧 English

Job description

About the role

The Clinical Trials Lead Site Coordinator will act as the primary liaison between sponsors or CROs and trial sites, ensuring smooth study execution and meeting enrollment targets.

Key responsibilities

Communicate feasibility responses and coordinate monitoring visits.
Track patient enrollment, manage study documents, and ensure timely data entry into EDC systems.
Report adverse events, protocol deviations, and handle investigational product accountability.
Support contract and budget negotiations, investigator payments, and prepare for audits or inspections.

Required profile

University degree in Life Sciences (pharmacy, nursing, or lab analytics preferred).
Minimum 3 years experience as a Study Coordinator or similar in clinical trials.
Upper‑Intermediate English and ability to work in a fast‑paced, global team.
Flexibility to work varied hours based on study procedures and patient visits.

Questions fréquentes

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Published 4 hours ago

Expires 1 month from now

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PSI CRO

Mendoza

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