Clinical Research Associates
693 open positions
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Clinical Research Associate (PhD Candidates) MedpaceCincinnati, Ohio today Conduct on-site and virtual monitoring visits at clinical research sites to ensure compliance with protocols, verify data accuracy, and manage investigational product accountability for pharmaceutical and medical device trials.
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Clinical Research Associate II / Senior CRA ErgomedParis, fr today Conduct 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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Clinical Data Reviewer Psi-CroRemote today Review clinical data remotely to identify errors, systemic issues, and trends related to data integrity, participant safety, and site performance.
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Experienced CRA - Real World Evidence with SSU experience IqviaBucuresti, Romania 1d Perform monitoring, site management, and Site Start-Up (SSU) activities for Real World Evidence (RWE) studies, ensuring sites conduct studies and report data in accordance with protocols and regulations.
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Senior Specialist, Clinical Research Monitoring EdwardsJapan-Tokyo 1d Monitoring clinical trials for medical devices and pharmaceuticals, ensuring compliance and data integrity from trial initiation to closure.
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Clinical Research Associate (CRA) BristolmyerssquibbField - Poland - PL $187k–$187k1d Field-based Clinical Research Associate ensuring quality, integrity, and compliance of clinical trial sites across all phases.
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Associé(e) de recherche clinique senior AbCelleraMontréal $0k–$0k1d Senior Clinical Research Associate acting as the primary liaison between AbCellera and clinical investigation sites to ensure patient safety, data integrity, and successful trial execution.
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Senior Clinical Research Associate AbbVieLos Angeles, CA, us 1d Senior Clinical Research Associate ensuring appropriate conduct of clinical trials, driving data integrity, compliance, and site performance for AbbVie's investigational drug/device trials.
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Senior Clinical Research Associate ClinChoiceRemote 1d Senior Clinical Research Associate supporting 2–3 clinical trials with site monitoring, study start-up, and data quality assurance for pharmaceutical, biotechnology, and medical device clients.
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(Senior) Clinical Research Associate↗ ICON PlcFrankfurt am Main, HE, DE 2d 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 (CRA) III (Hybrid)↗ Cvrx, Inc.Remote $127k–$142k2d Execute clinical trials for implantable medical devices by monitoring sites to ensure compliance with protocols, GCP, and regulations.
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Clinical Research Associate (CRA) / Klinische*r Monitor*in (d/w/m)↗ Charité - Universitätsmedizin BerlinRemote 2d Ensuring quality of execution for an international, randomized, multicenter clinical study in stroke research by planning and conducting risk-based monitoring.
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Assistant CRA ThermofisherRemote 2d Support Clinical Research Associates with site preparedness, logistical monitoring, and administrative tasks for clinical trials.
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Senior Clinical Research Associate MsdCHL - Santiago - Santiago (Calle Mariano), CL 2d Ensuring performance, quality, and compliance of clinical trial sites and protocols across the country.
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FSP - Assistant Clinical Research Associate (ACRA)↗ Thermo Fisher ScientificRemote 2d Support site preparedness, logistical monitoring, and remote review activities for clinical trials in collaboration with CRAs and Study Clinical Leads.
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(Senior) Clinical Research Associate IconGermany, Frankfurt 2d 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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Specialist, Regulatory and Site Activation - Mexico- Remote↗ Worldwide Clinical TrialsRemote 2d Subject matter expert and local point of contact for regulatory submissions, site activation, and maintenance for clinical research projects in Mexico.
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Central Monitor II (RBQM / KRI review Exp) JobgetherRemote 3d Support risk-based quality management across clinical research studies by reviewing study data, identifying trends, and assessing risks at study, country, and site levels.
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Clinical Trial Manager I - SCP↗ Syneos HealthKA, IN 3d Managing clinical sites and ensuring protocol compliance for oncology trials, including site selection, monitoring, and data integrity verification.
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サSingle Sponsor Clinical Research Associate II (Must have UK monitoring experience) UK only↗ サイネオス・ヘルスRemote 3d Conducts site qualification, monitoring, and close-out visits to ensure regulatory compliance and data integrity for clinical trials in the UK.
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サClinical Trial Manager I - SCP↗ サイネオス・ヘルスMH, IN 3d Managing clinical trial sites for oncology studies, ensuring protocol compliance, data integrity, and patient safety across the study lifecycle.
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Sr Clinical Research Associate II, Phase I↗ FortreaDurham, NC, US $100k–$100k4d Senior Clinical Research Associate providing high-standard care for Phase I clinical trial participants and managing study site operations.
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Senior CRA CoMindRemote 4d Senior Clinical Research Associate leading site monitoring and study oversight for a non-invasive neuromonitoring technology in hospital environments.
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