Clinical Research Associates
511 open positions
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Senior Clinical Research Associate Psi-CroRemote, US, us 1d Frontline communication with project stakeholders to ensure timelines, targets, and standards of clinical research projects across various therapeutic indications.
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Clinical Research Associate II AbbVieBrisbane, QLD, au 1d Primary sponsor point of contact for investigative sites, ensuring protocol compliance, patient safety, and successful recruitment/retention across diverse therapeutic areas.
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CRA II/ SCRA (NSW/ VIC/ QLD)↗ Syneos HealthRemote, AU 1d Conducts site qualification, initiation, monitoring, and close-out visits to ensure regulatory compliance and data integrity for clinical trials.
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Clinical Research Associate (Level II) and above↗ Thermo Fisher ScientificRemoto, PT 1d 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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Senior QA Auditor (GCP Audits) - Certified to Audit Sites in Italy IqviaMilan, Italy $48k–$48k1d Plan and conduct independent clinical (GCP) audits to assess compliance with regulations and guidelines for clinical research programs.
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Clinical Research Associate II (FSP) - Sydney FortreaSydney, New South Wales 1d Managing and monitoring clinical trials to ensure compliance with regulatory requirements and protect study subjects.
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Cra III / Scra I Avance ClinicalRemote 2d Conduct site feasibility, initiation, and monitoring visits to ensure clinical trials adhere to protocols, SOPs, and ICH GCP guidelines.
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FSP Experienced Clinical Research Associate (CRA II/Sr. CRA I) - Oncology ThermofisherRemote, Oregon, USA 3d Conduct remote or onsite monitoring visits to assess regulatory compliance, manage documentation, and ensure trial conduct per protocol and ICH GCP guidelines for oncology clinical trials.
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Site Engagement Liaison IreChennai, Tamil Nadu 3d Foster relationships with clinical trial sites to enhance engagement and contribute to the advancement of innovative treatments.
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Clinical Research Associate - PhD in Life Sciences MedpaceIrving (Dallas), Texas 3d Conduct on-site and remote monitoring visits at clinical research sites to ensure compliance with protocols, GCP, and regulatory requirements for drug and medical device development.
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Clinical Research Associate II / Senior CRA ErgomedParis, fr 4d 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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Senior Clinical Research Associate (Oncology) - UK (Remote) - FSP↗ ParexelRemote 4d Senior Clinical Research Associate ensuring clinical trial quality, data integrity, patient safety, and regulatory compliance at the site level for oncology studies.
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Clinical Research Associate II↗ ICON PlcChicago, IL, US $91k–$91k4d Primary liaison between investigational sites and the sponsor, conducting site visits to ensure compliance and monitor patient safety.
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サClinical Trial Manager - single sponsor - Germany↗ サイネオス・ヘルスRemote 4d Manage site oversight, clinical monitoring, and central monitoring deliverables for single-sponsor clinical trials to ensure patient safety, protocol compliance, and data integrity.
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Clinical Research Associate (CRA) BristolmyerssquibbField - Poland - PL $187k–$187k4d Field-based Clinical Research Associate ensuring quality, integrity, and compliance of clinical trial sites across all phases.
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サCRA↗ サイネオス・ヘルスRemote 4d Conduct on-site and remote clinical monitoring visits to ensure regulatory compliance, data integrity, and patient safety across drug development studies.
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Senior Specialist, Clinical Research Monitoring EdwardsJapan-Tokyo 4d Monitoring clinical trials for medical devices and pharmaceuticals, ensuring compliance and data integrity from trial initiation to closure.
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Associé(e) de recherche clinique senior AbCelleraMontréal $0k–$0k4d 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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