Clinical Research Associates
712 open positions
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Sr Cra - Georgia (Europe) - Home Based Syneos - Clinical and Corporate - ProdRemote 3mo Conducts site qualification, initiation, interim monitoring, management, and close-out visits to ensure regulatory compliance and data accuracy for clinical studies.
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Senior Clinical Research Associate Tech ObserverRemote 3mo Ensuring protocol and GCP compliance across clinical operations and monitoring projects for designated studies.
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CRA & CTA - Pharmaceutical Consultancy HaysValencia 3mo Clinical Research & Technical Associate responsible for on-site monitoring, regulatory compliance, and documentation support across the full lifecycle of observational studies.
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Clinical Research Associate S&YouTorino, Provincia di Torino $40k–$50k3mo Managing and monitoring national and international clinical studies to ensure compliance with Good Clinical Practice (GCP), study protocols, and applicable regulations.
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Site Visit Report Reviewer JobgetherIndia 3mo Reviewing clinical trial site visit reports to ensure compliance with regulatory standards and internal SOPs.
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Experienced CRA (multi-sponsor, multi-therapeutic, home-based and office-based positions available)↗ Medpace 3mo Conducting clinical monitoring visits at research sites to ensure protocol compliance, data accuracy, and patient safety across various therapeutic areas.
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Clinical Research Associate - Freelance TFS HealthScienceRemote 3mo Initiate, monitor (on-site and/or remote), and close out clinical study sites to ensure subject safety, data integrity, and regulatory compliance.
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Senior Clinical Research Associate (SCRA) Quotient SciencesNottingham, Nottinghamshire 3mo Build and lead an in-house clinical monitoring capability for early-phase (Phase I healthy volunteer and Phase 1b/2a patient) trials at Quotient sites in Nottingham and Miami, establishing risk-based, inspection-ready frameworks.
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Clinical Research Associate Phidealive SrlMilano, Provincia di Milano 3mo Monitoring clinical trials to ensure regulatory compliance and data accuracy for sponsors, biotech innovators, and investigators in Pharma, Biotech, Medical Device, and Food Supplement sectors.
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Clinical Research Associate Iqvia Rds. LimitedPerth CBD, Perth $100k–$100k3mo Ensure study sites are compliant and thriving to drive innovation and excellence in clinical research, specifically within Oncology trials.
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Clinical Research Associate 2 - IQVIA Biotech IqviaBarcelona 3mo Perform site monitoring visits (selection, initiation, monitoring, close-out) to ensure adherence to GCP and ICH guidelines for clinical trials in biotech and emerging biopharma.
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Lead CRA / Lead Monitor EPM Scientific BerlinRemote 3mo Lead Clinical Research Associate overseeing Phase I-IV international clinical trials, ensuring compliance and mentoring junior staff.
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Clinical Research Associate I ThermofisherRemote, Costa Rica 3mo Coordinate clinical monitoring and site management to ensure trial compliance with protocols, ICH-GCP guidelines, and regulations while guaranteeing subject rights and data reliability.
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Senior/Clinical Research Associate Precision for MedicineAustralia 3mo Senior Clinical Research Associate providing overall support to study sites and clinical project teams in oncology and rare disease trials, ensuring patient safety and data integrity.
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Senior Clinical Research Associate - FSP - Register Your Interest ParexelRemote 3mo Site management, monitoring, and close-out of clinical trial investigator sites to ensure patient safety and quality study execution.
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Freelance SCRA x4 - Serbian Speaking - 0.2 - 1.0 FTE ProPharma GroupNederland 3mo Conducting clinical monitoring for assigned protocols and investigational sites to ensure studies are conducted and documented in accordance with study protocols, SOPs, and GCP.
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Clinical Research Associate Ii - Sr Clinical Research Associate France H/F AllucentParis, Ile-de-France 3mo Lead monitoring activities for clinical trials, acting as the bridge between sponsor and site to ensure trial integrity and data quality.
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Clinical Research Associate, sponsor-dedicated Home Office - Deutschland FortreaRemote $0k–$0k3mo Managing all aspects of clinical study site selection and close-out for Phase I-III oncology trials in Germany.
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Clinical Operations Lead (Clinical Trial Manager) AlimentivFrankfurt 3mo Oversees clinical operations for a project at a regional or global level, managing deliverables, CRAs, and Investigator sites.
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Clinical Research Manager (Ass. Site Manager) Johnson and JohnsonBreda, Noord-Brabant 3mo Associate Site Manager serving as the primary contact between Sponsor and Investigational Site for clinical trials in phases 1b, 2 & 3 in the Netherlands and Belgium.
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Clinical Research Associate (sponsor dedicated) IreWarszawa, mazowieckie 3mo Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials to ensure protocol compliance, data integrity, and patient safety.
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Sr CRA I/II - FSP model - Poland - Homebased Syneos HealthRemote 3mo Conducts clinical trial site monitoring and management to ensure regulatory compliance and data integrity for drug development studies.
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Senior Clinical Research Associate (CRA)* ImmaticsRemote 3mo Ensure clinical trial site management and monitoring activities in compliance with GCP guidelines and regulations for novel PRAME immunotherapies.
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Clinical Research Associate II/Senior CRA CapijobnewRemote 3mo Conduct onsite monitoring visits, manage clinical study sites, and ensure data quality for Phase II/III trials in oncology, hemophilia, infectious diseases, and GI.
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Clinical Research Associate - Cell Therapy AstraZenecaRemote 3mo Monitoring and managing the initiation, conduct, and close-out of complex cell therapy clinical trials to ensure compliance and data integrity.
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Clinical Research Associate - sponsor dedicated - Amsterdam ICON Clinical ResearchNederland 3mo Design and analyze clinical trials, interpret complex medical data, and contribute to the advancement of innovative treatments and therapies.
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Senior Clinical Research Associate - Cardiometabolic, Oncology - Contractor - Germany Worldwide Clinical TrialsDeutschland 3mo Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials in cardiometabolic and oncology therapeutic areas.
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Clinical Research Associate VhirBarcelona 3mo Conduct monitoring visits and manage activities for clinical trials from Phase I to Phase IV, serving as the main communicator between sponsors and investigators.
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Clinical Research Associate ARC Regulatory LtdBelfast, Northern Ireland 3mo Act as a clinical site monitor for in vitro diagnostic (IVD) medical device clinical studies, ensuring compliance with protocols and regulations.
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Freelance Clinical Research Associate (Germany) Rho IncDeutschland 3mo Conducting site administration, monitoring, and feasibility assessments for clinical studies in Major Depressive Disorder.
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