Clinical Research Associate: Monitor Trials & Data Quality
Opis
OPIS is hiring a Clinical Research Associate to manage and monitor multi-country trials, ensuring adherence to ICH-GCP and regulatory standards.
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Desplácese hacia abajo y descubra qué habilidades, experiencia y cualificaciones académicas se necesitan.You will oversee site selection, initiation, monitoring, and close-out activities, while safeguarding data quality and patient safety.The role reports to the Clinical Project Manager and involves collaboration with sponsors, sites, and project teams.
xqysrnhRequires a scientific degree and 2+ years' CRA experience, with strong English and MS Office skills.
- ...OPIS is hiring a Clinical Research Associate to manage and monitor multi-country trials, ensuring adherence to ICH-GCP and regulatory standards. You will oversee... ...and close-out activities, while safeguarding data quality and patient safety.The role reports to the Clinical...DatosCalidadTrabajar en la oficina
- ...Novartis AG in Barcelona seeks a Lead Central Monitor to lead a team of Central Monitors and shape... ...strategies. You will collaborate across clinical, data, and risk-surveillance teams to protect patient safety, trial quality, and data integrity, translating complex signals...DatosCalidad
- ...OPIS s.r.l. is seeking a Clinical Research Associate to monitor and manage multi-country clinical trials, ensuring compliance with study... ...initiation, monitoring visits, data quality, and patient safety,... ...at least two years of CRA or trial monitoring experience (oncology...DatosCalidad
- ...working on complex clinical trials, specifically... ...aspects of study site monitoring including routine... ...integrity of the data submitted on Case... ...source document review.Monitor data for missing... ...contact for clinical trial supplies and other... ...and follow-up on Quality Control Visits (QC...DatosCalidad
50000 €/año
...The Clinical Research Associate is responsible for managing and monitoring clinical trials to ensure they are conducted in... ...activities, while ensuring data quality and patient safety.... ...completeness Monitor patient recruitment... ...’ CRA or clinical trial monitoring...DatosCalidadTrabajar en la oficina- ...Worldwide Clinical Trials is hiring an In-House Clinical Research Associate for Spain. This full-time, remote role supports virtual sites across Spain, including... ...Madrid and Catalonia. You will help ensure data quality, regulatory submissions, and TMF filing while coordinating...DatosCalidadTiempo completoRemoto
- ...Clinical Research Associate IQVIA Spain is looking for talented and... ..., initiation, monitoring and close-out visits... ...plan Evaluating the quality and integrity of site... ...form completion, and data query resolutions... ...Industry, and/or Clinical Trials environment Very good...DatosCalidadTrabajar en la oficinaInicio inmediatoHorario flexible
de 63600 a 118000 €/año
...leadership could transform how clinical trial risks are identified,... ...portfolio? As Lead Central Monitor, you will lead and develop... ...protect patient safety, trial quality, and data integrity. Working across clinical... ...pharmaceutical or contract research organisation experience,...DatosCalidadContratoTrabajo híbridoHorario flexible50000 €/año
Clinical Research Associate manages and monitors clinical trials, ensuring compliance with protocols, regulations, and data quality. Responsibilities include site selection, initiation, monitoring, and close-out.DatosCalidad- ...Clinical Research Associate II position in Barcelona supporting... ...dedicated clinical trials. The role involves monitoring activities, ensuring... ..., managing data integrity, and collaborating... ...safety throughout trial process... ...to maintain high-quality clinical data Contribute...DatosCalidad
- ...IQVIA Biotech seeks a Clinical Research Associate to conduct site monitoring across multiple therapeutic... ...managing clinical trial sites, ensuring regulatory... ...enrollment and data quality, and collaborating with... ...communication with study sites Monitor study progress...DatosCalidad
- ...ICON Strategic Solutions seeks a Clinical Research Associate II for a home-based role in Barcelona. You will monitor trials, ensure data integrity, and support study delivery in a... ...collaboration with investigators and high-quality clinical data management. #J-*****-...DatosCalidadDesde casa
- ...The Senior Clinical Research Associate II is responsible... ...management, site monitoring and close-out... ...clinical trials investigator sites... ...safety and quality study execution... ...in a clinical trial. JOB RESPONSIBILITIES... .... Monitor site level AEs... ...issues Resolve data queries within...DatosCalidadRemoto
- ...Clinical Research Associate Home based Barcelona At ICON Strategic... ...and analyse clinical trials, interpreting complex medical data, and contribute to the... ...contribute to clinical trial monitoring activities, taking... ...queries to maintain high-quality clinical data....DatosCalidadTrabajo remotoAutónomoDesde casa
- ...Clinical Research Associate Home based BarcelonaAt ICON Strategic Solutions... ...and analyse clinical trials, interpreting complex medical data, and contribute to... ...to clinical trial monitoring activities, taking responsibility... ...to maintain high-quality clinical data....DatosCalidadAutónomoDesde casa
- ...Clinical Research AssociateIQVIA Spain is looking for talented... ...selection, initiation, monitoring and close-out... ...recruitment planEvaluating the quality and integrity of site... ...form completion, and data query resolutionsCollaborating... ..., and/or Clinical Trials environmentVery good...DatosCalidadTiempo completoInicio inmediatoHorario flexible
- ...working on complex clinical trials, specifically... ...aspects of study site monitoring including routine... ...integrity of the data submitted on Case... ...source document review.Monitor data for missing... ...contact for clinical trial supplies and other... ...and follow-up on Quality Control Visits (QC...DatosCalidad
- ...intelligence and clinical research organisation... ...Research Associate II to join our... ...analyzing clinical trials, interpreting... ...complex medical data, and... ..., initiation, monitoring, and close-out... ...throughout the trial process.Collaborating... ...maintain high-quality clinical to the...DatosCalidadTiempo completo
- ...implement them with quality and excellence.... ...We are Worldwide Clinical Trials, and we are a... ...way. Clinical Research Associates (CRAs) play a vital... ...on every clinical trial. Our leaders are... ..., interim monitoring, site management,... ...and veracity of data. Review CRFs using...DatosCalidadInterinoTrabajar en la oficina
- ...Sr. Clinical Research Associate ICON plc is a world-leading healthcare... ...managing clinical trial activities to ensure... ...clinical trials by ensuring data integrity,... ...You Will Be Doing: Monitoring clinical trial sites... ...success depends on the quality of our people. That’s...DatosCalidadTrabajo remotoAutónomo
- ...implement them with quality and excellence... ...are Worldwide Clinical Trials, and we are a... ...Clinical Research Associates (CRAs) play a... ...every clinical trial. All CROs will... ..., interim monitoring, site management... .... Assess, monitor, and train study... ...veracity of data. Review CRFs...DatosCalidadInterinoTrabajar en la oficinaRemoto
- ...Alira Health Clinical team. The... ...site monitoring responsibilities... ...for clinical trials; as well as... ...compliance and quality. The Sr... ...house CRAs, EU: Associate Director of... ...clinical trial monitoring related... ...of CRF data through meticulous... ...of clinical research, ICH GCP and...DatosCalidadTiempo completoInterinoContratoRemoto
- ...currently seeking Senior Clinical Research Associates in Spain to... ...collaborative and quality-focused environment.... ...growth: You will monitor and own the progress... ...appropriately sized clinical trials, and support clinical... ...in English. Any data provided as a part of...DatosCalidadDesde casaInicio inmediatoTurno de noche
- ...Overview The Clinical Research Associate at Medpace is offering the unique... ...Manager, Clinical Trial Manager; Sign on... ...qualification, initiation, monitoring, and closeout visits... ...case report form data, including informing... ...based on expertise, quality, capabilities, reliability...DatosCalidadContratoTrabajar en la oficinaDesde casaHorario flexible
- ...Clinical Research Associate Home based Barcelona At ICON Strategic... ...and analyse clinical trials, interpreting complex medical data, and contribute to the... ...contribute to clinical trial monitoring activities, taking... ...queries to maintain high-quality clinical data....DatosCalidadAutónomoDesde casa
- ...Senior Clinical Research Associate Home based Spain At ICON Strategic... ...and manage clinical trial activities to ensure... ...lead on clinical trial monitoring tasks requiring technical... ..., with a focus on quality and continuous improvement... ...timely and accurate data collection and...DatosCalidadAutónomo
de 55000 a 65000 €/año
...CRA Spain The Senior Clinical Research Associate (Sr CRA) is a key member... ...conducts site monitoring activities, oversees clinical trial execution, and ensures... ...protocol compliance and quality throughout the study life... ...Ensures integrity of CRF data through meticulous...DatosCalidadInterinoContratoRemoto- ...life balance, and a quality-focused,... ...seeking a Senior Clinical Research Associate (Senior CRA) to join... ...travel to clinical trial sites is required... ...responsible for site monitoring activities,... ...Conduct source data verification and... ...Manager, Remote Monitor, Site Monitoring,...DatosCalidadTiempo completoEmpleo permanenteContratoTrabajar en la oficinaRemoto
de 63600 a 118000 €/año
...Lead Central Monitor role at Novartis in Barcelona, Spain, focusing on developing monitoring strategies and leading a team to ensure patient safety, data integrity, and trial quality in clinical programs. Requires 7+ years of pharma/CRO experience and GCP/ICH knowledge...DatosCalidad- ...Clinical Trial Posting Manager Develops or contributes to the development of the organization... ...Bayer's Clinical Trials at high level quality by fully complying to the related Quality... ...date and consistent Clinical Trial Posting data on required company owned and public...DatosCalidadTiempo completo
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