Clinical Research Associates
714 open positions
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Junior Clinical Research Associate (CRA) – Transition Opportunity for CRCs & Junior CRAs | Brisbane Thermo-Fisher-ScientificBrisbane, Queensland 1mo Perform clinical monitoring and site management for sponsor-driven trials, ensuring protocol and regulatory compliance.
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Senior / Clinical Research Associate IqviaMelbourne, New South Wales 1mo Perform site monitoring and management to ensure clinical studies are conducted per protocol and regulations, managing data integrity and site operations.
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Sr Clinical Research Associate I Sydney, Melbourne, or Perth FortreaSydney, New South Wales 1mo Senior Clinical Research Associate responsible for site monitoring, site management, and registry administration for clinical studies.
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Study Start Up Associate IreRemote 1mo Act as a strategic liaison between ICON and key investigator sites to strengthen relationships and support study performance.
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Senior Clinical Research Associate Psi-CroShanghai/Beijing, cn 1mo Senior Clinical Research Associate performing full-cycle site monitoring, managing trial supplies, and leading regional project activities for Phase II/III clinical studies.
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Clinical Research Associate II AbbVieSofia, Sofia City Province, bg 1mo Partner with investigative sites and staff to ensure appropriate conduct of clinical trials, driving data integrity, compliance, and study performance.
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FSP Clinical Research Associate II ThermofisherRemote, Romania 1mo Coordinate clinical monitoring and site management to ensure trials comply with protocols, ICH-GCP guidelines, and regulations while guaranteeing subject rights and data reliability.
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Specialist, Quality Assurance CareaccessRemote $70k–$90k1mo Ensure quality and compliance of clinical work at traditional and decentralized trial sites through audits, CAPA management, and regulatory document reviews.
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Clinical Research Associate II or Sr ParexelSão Paulo, Estado de São Paulo 1mo Monitor clinical trial sites through on-site and remote visits to ensure high-quality study execution and compliance.
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Attaché de Recherche Clinique Biopharma (H/F) AstraZenecaFrance - La Defense 1mo Monitor international clinical studies ensuring protocol, regulatory, and timeline compliance while representing AstraZeneca's ethics to investigators.
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Clinical Research Monitor MedtronicMaastricht, Limburg, Netherlands $53k–$53k1mo Monitor clinical research at investigational sites to ensure compliance with study protocols, regulatory requirements, and ethics committee policies.
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サSponsor dedicated Sr CRA I Oncology Phase I - Barcelona/Madrid↗ サイネオス・ヘルスRemote 1mo Senior Clinical Research Associate (CRA) managing oncology Phase I clinical trial sites in Spain, ensuring protocol compliance, data integrity, and patient safety.
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Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)↗ MedpaceBoston, MA, US 1mo Transform a Clinical Research Coordinator into a fully resourced Clinical Research Associate (CRA) to conduct qualification, initiation, monitoring, and closeout visits at research sites.
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Sr Clinical Research Associate Contractor (Australia)↗ AllucentBrisbane, QLD, AU 1mo Independently monitor investigational sites to ensure clinical studies are performed according to trial protocols, SOPs, and GCP regulations.
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Clinical Research Associate II↗ ICON Strategic Solutions 1mo Conduct clinical trial monitoring activities including site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance, data integrity, and patient safety.
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Sponsor dedicated Sr CRA I Oncology Phase I - Barcelona/Madrid↗ Syneos HealthMadrid, MD, ES 1mo Senior Clinical Research Associate leading site qualification, monitoring, and management for oncology Phase I clinical trials.
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サCRAII/ SCRAI↗ サイネオス・ヘルスRemote 1mo Conducts site qualification, initiation, monitoring, and close-out visits to ensure regulatory compliance and data integrity for clinical trials.
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Clinical Research Associate↗ Dr. Reddy's LaboratoriesTS, IN 1mo Manage clinical investigational sites to ensure accurate, timely, and consistent data reaches clinical teams; oversee site initiation, monitoring, and compliance.
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Clinical Research Associate I↗ Beone MedicinesRemote 1mo Conduct clinical site visits and manage study sites to ensure protocol compliance, data quality, and patient safety for oncology trials.
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