Clinical Research Associates
701 open positions
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Entry-Level Clinical Research Associate (remote) - Clinical Study Coordinator Experience Required MedpaceRemote 12d Conduct on-site and virtual monitoring visits at clinical research sites to ensure protocol compliance, data accuracy, and patient safety for drug and medical device development.
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Auditor - GCP CslAmericas, US-PA, King of Prussia, CSL Behring 13d 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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Clinical Research Associate II↗ ICON PlcChicago, IL, US $91k–$91k13d Primary liaison between investigational sites and the sponsor, conducting site selection, initiation, routine monitoring, and close-out to ensure compliance and data quality.
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Clinical Research Associate II IconRemote 13d Monitor Phase I–III clinical trials to ensure compliance with ICH-GCP and regulatory requirements, managing studies across multiple therapeutic areas in France.
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Clinical Research Associate (CRA) MsdAUS - New South Wales - Macquarie Park, AU 13d Primary site contact and manager responsible for protocol compliance, data integrity, and subject safety across clinical trial phases.
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Senior CRA - Germany↗ Syneos HealthHome Office, DE 13d Senior Clinical Research Associate responsible for site qualification, monitoring, and management to ensure regulatory compliance and data integrity in clinical trials.
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Clinical Research Compliance Specialist↗ Alliance Clinical NetworkRochester, NY, US 13d Monitor protocol and regulatory compliance for clinical research studies, review research data for accuracy, and manage documentation and milestones.
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FSP CRA ─ with Sign-on Bonus ThermofisherRemote, Korea, Republic of 13d Ensure clinical studies at investigator sites comply with protocols, ICH GCP, and local laws to protect subject rights and ensure data accuracy.
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サSenior CRA - Germany↗ サイネオス・ヘルスRemote 13d Senior Clinical Research Associate ensuring regulatory compliance and data integrity for clinical study sites in Germany.
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Experienced Clinical Research Associate (CRA II/Sr CRA) - AR, KS, LA, MO, OK, TX - Multiple Therapeutic Areas Available↗ Thermo Fisher ScientificTX, US 13d 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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Lead Clinical Research Associate (Lead CRA)↗ Armata PharmaceuticalsMarina del Rey, CA, US $112k–$140k13d 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–$100k13d 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 13d Senior Clinical Research Associate ensuring regulatory compliance and data integrity across clinical study sites in Germany.
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サSr CTM↗ サイネオス・ヘルスRemote 13d 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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Senior Clinical Research Associate Worldwide Clinical TrialsBrasil 15d Manage research activities at clinical trial sites, overseeing study initiation, maintenance, and closure while ensuring regulatory compliance.
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Clinical Research Associate↗ Orca BioRemote, US 16d Monitor clinical trials for blood cancer cell therapies at investigative sites to ensure compliance with protocols and regulations.
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CRC III↗ Dynamed Clinical Research LpTomball, TX, US 16d Ensure quality research and data collection at assigned clinical trial sites in accordance with sponsor protocols, FDA regulations, and ICH/GCP guidelines.
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GCP Auditor (Freelance) ErgomedRemote 16d Planning, conducting, and reporting Good Clinical Practice (GCP) audits for pharmaceutical and biotechnology companies to ensure regulatory compliance and patient safety.
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サCRA II (Oncology), Full Service, Thailand (remote)↗ サイネオス・ヘルスRemote 17d Clinical Research Associate II performing site qualification, monitoring, and management for oncology clinical trials in Thailand.
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Senior Clinical Research Associate - West Coast/Oncology↗ SystimmuneRemote $110k–$110k17d Manage and oversee clinical study sites for oncology trials to ensure data quality and patient safety in accordance with ICH-GCP guidelines.
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In-House Clinical Research Associate (Contract)↗ 4d Molecular TherapeuticsEmeryville, CA, US $125k–$125k17d In-house Clinical Research Associate supporting Phase 3 clinical trial execution, site management, and regulatory compliance for late-stage biotech therapeutics.
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In-House Clinical Research Associate↗ The Emmes Company, LLCRemote 17d Assist with operational activities supporting site management and monitoring of clinical studies/trials, ensuring compliance with protocols and regulatory requirements.
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Clinical Research Associate II (Contract based) Psi-CroLisbon, Lisbon, pt 17d Conduct onsite monitoring visits, manage clinical sites, and ensure data compliance for Phase II/III clinical research projects in Inflammatory Bowel Diseases.
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Senior Clinical Research Associate AbbVieMinato City, Tokyo, jp 18d Primary Sponsor point of contact for investigative sites, ensuring appropriate trial conduct, data integrity, and compliance while driving patient recruitment and retention.
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In-House Clinical Research Associate↗ Terumo AorticInchinnan, SCT, GB 19d Oversee remote site management, centralized monitoring, and data review to ensure compliant delivery of clinical trials.
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