Clinical Research Associates
550 open positions
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CRA II or Sr CRA (sponsor dedicated) - Min 3 years of previous monitoring exp - CDMX Syneos HealthMéxico 1mo Conduct clinical site monitoring, qualification, and management to ensure regulatory compliance and data integrity for biopharmaceutical studies.
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Sr. CRA Level 1 FSO ThermoFisher ScientificBrasil 1mo Senior Clinical Research Associate conducting risk-based monitoring, site initiation, and audit readiness for clinical trials across pharmaceutical and biotech sectors.
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Lead Clinical Research Associate Psi-CroToronto, ON, ca 1mo Oversees clinical trial monitoring, site management, and data integrity for global Phase I-III studies, ensuring regulatory compliance and patient enrollment targets.
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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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Clinical Research Associate 2 AbbVieWarsaw, Masovian Voivodeship, pl 1mo Monitors clinical investigative sites to ensure successful execution of protocols, adherence to regulations, and quality standards for Phase 1-4 studies.
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GCP Clinical Auditor II (remote US) ThermofisherRemote $60k–$60k1mo Lead and perform complex internal and external audits to ensure compliance with GCP, quality assurance processes, and regulatory guidelines for clinical research projects.
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Senior Clinical Research Associate (Argentina)↗ Precision for MedicineBuenos Aires, Buenos Aires Province, Argentina 1mo Senior Clinical Research Associate managing complex clinical trials across Argentina, ensuring patient safety, data quality, and regulatory compliance.
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Senior Clinical Research Associate - FSP ParexelBrasil 1mo Manage assigned clinical trial investigator sites from activation through close-out to ensure patient safety, quality execution, and compliance with GCP and client standards.
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FSP Sr. Clinical Research Associate II - NYC Metro or PHL - Onc↗ FortreaNew York, United States $125k–$125k1mo Senior Clinical Research Associate ensuring protocol adherence, patient safety, and data integrity for oncology clinical trials.
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Risk and Central Monitoring Manager - Argentina/Mexico - Remote↗ Worldwide Clinical TrialsRemote 1mo Coordinates cross-functional risk management and central monitoring activities for assigned clinical trials to ensure quality and consistency.
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Senior Clinical Research Associate MsdMYS - Selangor - Petaling Jaya (Ascent Paradigm), MY 1mo Ensure performance and compliance of assigned clinical trial protocols and sites within the country, serving as the primary site contact and manager throughout all study phases.
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Clinical Research Associate II IconMalaysia, Kuala Lumpur 1mo Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials to ensure protocol compliance, data integrity, and patient safety.
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Clinical Research Associate (Biomedical Engineering Candidates) MedpaceIrving (Dallas), Texas 2mo Conduct qualification, initiation, monitoring, and closeout visits at research sites to ensure compliance with protocols and regulatory requirements for pharmaceutical and medical device development.
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Senior Clinical Research Associate↗ Tigermed 2mo Manage clinical study sites from selection to close-out, ensuring data quality, safety reporting, and regulatory compliance for Tigermed or sponsor studies.
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Senior Clinical Research Associate ErgomedRemote 2mo Conducts on-site or remote monitoring visits (Pre-Study, Initiation, Interim, Close-Out) to ensure investigational sites and staff are adequate for clinical study conduct.
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