Clinical Research Associates
712 open positions
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Clinical Research Associate 2 – Multisponsor – South of Spain IqviaRemote 3mo Conduct independent site monitoring, selection, initiation, and close-out visits for clinical trials to ensure protocol adherence and data integrity.
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Sr. Clinical Research Associate CareDxRemote $100k–$100k3mo Ensuring the integrity, quality, and compliance of clinical trials for transplant patients through site monitoring and data management.
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Unblinded CRA I based in Frankfurt or Ruhr Area FortreaDeutschland 3mo Perform unblinded monitoring activities and Investigational Product oversight at clinical trial sites in Germany to ensure protocol compliance, data integrity, and patient safety.
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FSP Senior CRA ThermofisherRemote 3mo Conduct remote and on-site clinical monitoring for complex oncology and cell/gene therapy studies to ensure protocol compliance, data accuracy, and site management.
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Clinical Research Associate III (Remote) NovartisSanto Amaro, Bahia 3mo Deliver high-quality clinical trials for innovative therapies by managing site partnerships, monitoring data integrity, and ensuring regulatory compliance across Phase One to Four studies.
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Freelancer / Clinical Research Associate (CRA) Scirent Clinical Research and ScienceParis, Ile-de-France 4mo Conducting clinical monitoring visits, reviewing source data, and ensuring accurate reporting of adverse events for cardiovascular drug and device trials.
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Senior Clinical Research Associate - Oncology, CNS, Rare Disease - UK Worldwide Clinical TrialsUK 4mo Ensuring clinical research programs are executed with quality and excellence by managing site visits, monitoring protocol adherence, and verifying data for oncology, CNS, and rare disease trials.
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CRA I - FSP - France ThermoFisher ScientificFrance 4mo Conduct remote and on-site clinical monitoring visits to assess protocol and regulatory compliance, manage documentation, and ensure audit readiness for clinical trials.
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Senior Clinical Research Associate (Oncology Experience Required) - UK - FSP ParexelRemote 4mo Senior Clinical Research Associate ensuring data integrity, compliance with ICH GCP, and protocol adherence at clinical trial sites.
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Sr CRA - Oncology experienced required IreReading, Berkshire 4mo Overseeing and managing clinical trial activities to ensure adherence to protocols, regulatory requirements, and GCP standards while ensuring data integrity and participant safety.
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Sr CRA - Oncology experienced required ICON Clinical ResearchUK 4mo Overseeing and managing clinical trial activities to ensure adherence to protocols, regulatory requirements, and GCP standards, focusing on data integrity and participant safety.
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Clinical Research Associate II/III - SA NovotechProspect, Prospect Area 4mo Ensuring rights and wellbeing of trial participants are protected and reported trial data are accurate, complete, and verifiable from source documents.
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Clinical Research Associate (I) and (II) Novo Nordisk PharmaceuticalsThe Rocks, Sydney 4mo Vital link between Novo Nordisk, clinical trial sites, and cross-functional study teams ensuring patient safety, data integrity, and protocol compliance across assigned clinical trial sites in Australia.
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Clinical Research Associate (CRA) EvidenzeLanza, Milano 4mo Conduct clinical trials by performing site visits, monitoring compliance, and managing study documentation to ensure data integrity and regulatory adherence.
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Clinical Research Associate / Klinischer Monitor (m/w/d) Iges GruppeRemote 4mo Monitoring clinical trials for pharmaceuticals, medical devices, and digital health apps across Europe by visiting study sites and ensuring data validity.
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Clinical Research Associate (CRA) – German & French Speaking Clinsearch - Cast® - Edclin™Malakoff, Antony 4mo Monitor clinical trial sites in Germany and France to ensure compliance with Good Clinical Practice (GCP) and support communication with Institutional Review Boards.
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Senior Clinical Research Associate Alira HealthRemote 4mo Senior Clinical Research Associate conducting site monitoring, oversight, and leadership for clinical trials to ensure compliance and quality.
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Sr. Clinical Research Associate (Germany) AllucentKöln, Nordrhein-Westfalen 4mo Independent monitoring of investigational sites to ensure clinical studies are performed according to trial protocol and in compliance with regulations and GCP.
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Clinical Research Associate II AvaniaDeutschland 4mo Establish, maintain, and support clinical trials by verifying subject rights, data accuracy, and protocol compliance through site monitoring.
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Clinical Research Associate - Germany LinicalMoosach, München 4mo Manage investigative sites across Germany to ensure clinical trials are conducted in accordance with study protocols, ICH-GCP, and regulatory requirements.
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