Clinical Research Associates
882 open positions
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Histologist IconUnited States of America 4d Train into a Clinical Research Associate (CRA I) role to deliver clinical trial monitoring work, ensuring compliance and patient safety across clinical programmes.
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Sr. Clinical Research Associate - Early Phase Studies↗ Thermo Fisher ScientificLas Vegas, NV, US 4d Independently monitor investigational sites for Phase I and early-phase clinical pharmacology studies, ensuring protocol compliance, participant safety, and data integrity.
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Clinical Research Associate - West Coast↗ Tg Therapeutics, Inc. 4d Monitor and manage clinical research sites for Phase I-IV studies to ensure compliance with protocols, SOPs, and regulatory requirements.
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Sr. OPHTHALMOLOGY CRA - Canada↗ SrgRemote 4d Clinical Research Associate supporting a portfolio of retina-focused clinical studies in Canada, managing site activities and ensuring protocol compliance.
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Sr. Bilingual Clinical Research Associate↗ ICON Strategic SolutionsMontreal, Quebec, Canada 4d Ensuring regulatory, ICH-GCP, and protocol compliance at clinical trial sites through on-site and remote monitoring, source data verification, and management of investigational products.
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Clinical Research Associates (CRA)↗ University of UtahSalt Lake City, UT, US $60k–$90k4d Monitor all aspects of clinical research to ensure trial activities are conducted, recorded, and reported in accordance with protocols, SOPs, GCPs, and regulatory requirements.
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Senior Clinical Research Associate - CNS - Immunology - Germany↗ Worldwide Clinical TrialsDE 4d Senior Clinical Research Associate managing CNS/Immunology clinical trials in Germany, ensuring site compliance, patient safety, and data quality from initiation to close-out.
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SrCRA ThermofisherRemote, Slovakia 4d Senior Clinical Research Associate conducting remote and on-site monitoring of investigator sites to ensure protocol and regulatory compliance, manage documentation, and guarantee subject rights and data reliability.
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Senior Clinical Research Associate↗ Atlas SearchColorado, United States 4d Partner with a growing, high-quality and innovative team to enable quality and on-time execution of clinical trials.
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CRA II - Oncology Biotech↗ SystImmunePrinceton, NJ $80k–$110k4d Manage and oversee assigned clinical study sites to ensure data quality and patient safety in accordance with ICH-GCP guidelines and local regulations.
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Clinical Research Associate↗ Alira Health $95k–$130k4d Senior Clinical Research Associate providing oversight, leadership, and guidance for clinical trial site monitoring to ensure compliance and quality.
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Associate I Clinical Research↗ AbbottAlameda, CA 4d Clinical Research Associate ensuring quality, accuracy, and integrity of clinical trial data throughout the full lifecycle of multiple clinical trials.
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Clinical Research Associate (CRA)- Dermatology & Aesthetics Studies↗ ConfidentialRemote 4d Conduct on-site monitoring for Phase 2 drug and medical device studies in dermatology and aesthetics across 5–6 sites in the South/Southeast US.
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Government Sector Sr. In-House CRA↗ Emmes GroupRemote 4d Senior In-House Clinical Research Associate supporting site management and monitoring of clinical studies/trials, ensuring compliance with protocols and regulatory requirements.
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Clinical Research Associate↗ ICON PlcGA, US 4d Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials in cardio and obesity areas.
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Clinical Research Associate II↗ Psi CroMadrid, Community of Madrid, Spain 4d Frontline communication with project stakeholders to ensure timelines, targets, and standards of clinical research projects across various therapeutic indications.
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Graduate Clinical Research Associate (CRA)↗ NovotechSouth San Francisco, CA $60k–$65k4d Entry-level training role for aspiring Clinical Research Associates (CRAs) to build foundational skills in clinical trial conduct, site management, and regulatory compliance through an 8-week program.
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Clinical Research Associate↗ MedpaceAdelaide, South Australia, Australia 4d Conduct qualification, initiation, monitoring, and closeout visits for research sites to ensure compliance with protocols and regulations.
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Clinical Research Associate (CRA)↗ ClinixirBangkok City, Thailand 4d Junior Clinical Research Associate supporting Phase I–IV clinical trials through site management, monitoring visits, and regulatory compliance.
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Risk Manager (Clinical Research)-India↗ Indero (formerly Innovaderm)Delhi, Delhi, India 4d Develop and execute risk-based monitoring strategies to ensure data quality and integrity in clinical research projects.
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Clinical Research Associate II AbbVieMaidenhead, ENGLAND, gb 4d Field-based Clinical Research Associate ensuring appropriate conduct of clinical trials, driving data integrity, compliance, and study performance for AbbVie's pipeline.
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Experienced Clinical Research Associate- Oncology- Israel IqviaNetanya, Israel 5d Conduct site qualification, initiation, monitoring, and close-out visits for oncology clinical trials to ensure patient safety, data integrity, and protocol compliance.
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Clinical Research Associate↗ Medical University of South Carolina 5d Independent site monitor ensuring clinical trial compliance, data accuracy, and subject protection at Canadian hospital sites.
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Clinical Research Associate 1↗ Hologic, Inc.San Diego, CA $74k5d Conducts site monitoring and management activities for clinical trials, ensuring protocol adherence and data accuracy.
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Site Manager of Clinical Research↗ Dm Clinical ResearchAlbuquerque, NM, US 5d Ensure quality clinical research is conducted at assigned investigative sites in accordance with sponsor protocols, FDA regulations, and ICH/GCP guidelines to provide the best quality data to the sponsor.
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Analista de Pesquisa Clinica Pleno , Saude Humana , 1 vaga↗ União Química Farmacêutica NacionalSão Paulo, São Paulo, Brazil 5d Planning, conducting, and monitoring clinical studies and bioequivalence/biodisponibility studies to ensure compliance with protocols, regulations, and GCP.
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Clinical Research Associate↗ Piper Companies 110k–125k5d Conduct independent clinical monitoring visits to ensure pharmaceutical/biotechnology studies are conducted in compliance with ICH-GCP guidelines and regulatory requirements.
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Clinical Research Assoc III↗ Tranquil Clinical Research and Consulting ServicesWebster, TX 5d Manage and oversee clinical trials, ensuring compliance with regulatory requirements and company standards while monitoring study sites and ensuring data integrity.
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Clinical Research Associate II – West Coast USA↗ Linical $95k–$135k5d Conduct site qualification, initiation, monitoring, and close-out visits for complex clinical studies to ensure participant safety and data integrity.
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