Clinical Research Associates
547 open positions
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CRA I/II/ Sr CRA - FSP - UK ThermofisherRemote, United Kingdom 15d Conduct independent on-site clinical monitoring to ensure quality and accuracy of clinical trial data across multi-national projects.
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Senior Central Monitor (Remote)↗ ProPharma GroupRemote 15d Central monitoring associate supporting clinical monitoring teams by utilizing centralized data and reporting tools to ensure study delivery within timelines.
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サCRA II_Barcelona_Sponsor dedicated. Experience in onco-hematology, and gynecologic oncology clinical trials.↗ サイネオス・ヘルスRemote 15d Clinical Research Associate II performing site qualification, monitoring, and management for oncology and gynecologic oncology clinical trials.
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サCRA II_Madrid_Sponsor dedicated. Experience in oncology clinical trials (lung).↗ サイネオス・ヘルスRemote 15d Clinical Research Associate II performing site qualification, monitoring, and management for oncology clinical trials (specifically lung cancer) in a sponsor-dedicated role.
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Clinical Research Associate↗ ICON PlcBlue Bell, PA, US 15d Conduct clinical trial monitoring activities including site qualification, initiation, monitoring, and close-out visits for cardio and obesity trials.
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RWE - Site Mgr 2↗ IqviaRemote 15d Remote site monitoring and management to ensure clinical study compliance with protocols and regulations.
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CSP Oversight Specialist II IovancebiotherapeuticsRemote $110k–$110k15d Ensuring clinical service providers (CSPs) are qualified, assessed, and compliant with GCP and company policies to support Iovance's TIL therapy development.
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Senior Clinical Research Associate - Contract ClinChoiceRemote 15d Senior Clinical Research Associate monitoring oncology and medical device clinical trials, specifically focusing on therapeutic medical devices and HIFU therapy.
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Clinical Research Associate II Psi-CroAnkara, Ankara, tr 15d Frontline communication with project stakeholders to ensure timelines, targets, and standards of clinical research projects across various therapeutic indications.
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Senior Clinical Research Associate EPM Scientific BerlinRemote 15d Conducting independent monitoring visits and managing investigator sites for innovative medical device clinical studies across Germany and Europe.
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Experienced Clinical Research Associate (CRA II/Sr CRA) - Montreal, QC Canada - Bilingual↗ Thermo Fisher ScientificAB, CA 16d Conduct remote and on-site clinical monitoring to ensure protocol and regulatory compliance, manage site processes, and guarantee data reliability for pharmaceutical and biotech clinical trials.
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Virtual CRA Info Session - 11.4.2026 (Clinical Research Coordinator Experience) MedpaceUnited States 16d Conduct on-site and virtual monitoring visits at clinical research sites to ensure protocol compliance, data accuracy, and patient safety for biopharma and medical device trials.
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Clinical Research Compliance Specialist↗ Alliance Clinical NetworkRochester, NY, US 17d Monitor protocol and regulatory compliance for clinical research studies, review research data for accuracy, and manage documentation and milestones.
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Senior Clinical Research Associate IconRemote 17d Oversee and manage Phase I–III clinical trial activities to ensure compliance with protocol, regulatory requirements, and industry standards.
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Lead Clinical Research Associate (Lead CRA)↗ Armata PharmaceuticalsMarina del Rey, CA, US $112k–$140k17d Operational lead for a team of Clinical Research Associates providing oversight of clinical site monitoring activities across Phase II and III trials for antimicrobial therapies.
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FSP Clinical Research Associate 2 - West, Central, and South Regions↗ FortreaDurham, NC, US $100k–$100k17d Conduct clinical site monitoring, manage study data integrity, and ensure patient safety and protocol adherence across clinical trials.
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サSenior CRA - Germany↗ サイネオス・ヘルスRemote 17d Senior Clinical Research Associate ensuring regulatory compliance and data integrity across clinical study sites in Germany.
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Auditor - GCP CslAmericas, US-PA, King of Prussia, CSL Behring 17d Execute global GCP audits of clinical investigator sites, CROs, and E-System providers to ensure clinical trial data accuracy and regulatory compliance.
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Sr CTM↗ Syneos HealthRemote, US 17d Oversees site management, clinical monitoring, and central monitoring deliverables to ensure patient safety, protocol compliance, and data integrity for clinical trials.
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サSr CTM↗ サイネオス・ヘルスRemote 17d Oversees site management, clinical monitoring, and central monitoring deliverables to ensure patient safety, protocol compliance, and data integrity for clinical trials.
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(Junior) Clinical Trials Manager Site Management und Monitoring Oversight VertanicalGräfelfing/Munich 17d Central point of contact for study sites, responsible for site selection, coordination of outsourced start-up/monitoring/close-out activities, and oversight of monitoring plans for a cannabinoid-based pain treatment drug.
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Clinical Research Associate (CRA) MsdAUS - New South Wales - Macquarie Park, AU 17d Primary site contact and manager responsible for protocol compliance, data integrity, and subject safety across clinical trial phases.
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サSenior CRA - Germany↗ サイネオス・ヘルスRemote 17d Senior Clinical Research Associate ensuring regulatory compliance and data integrity for clinical study sites in Germany.
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Senior Clinical Research Associate Worldwide Clinical TrialsBrasil 19d Manage research activities at clinical trial sites, overseeing study initiation, maintenance, and closure while ensuring regulatory compliance.
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