Clinical Research Associate
Há 7 dias
As a Clinical Research Associate (CRA) you will be dedicated to one of our global Healthcare clients who have a strong legacy of innovation and leading the way within a specialist therapeutic area. **Responsibilities**: - Perform all type of visits from site feasibility to close out visits according to plan, document actions and follow up on action plans - Train and guide site staff in safety information handling, systems, protocol and trial procedures to minimize protocol deviations - Proactive use of EDC and other data source systems for preparation and conduct on site visits as well as source data verification in collaboration with data management/logistics team - Identify potential risks and proactively take action to prevent or mitigate - Collaborate with Data Management/logistics in resolving queries - Assist to ensure data cleaning cycle timelines are met in accordance with the Data Flow Plan - Motivate and build strong relations with site personnel to assist the sponsor in being their preferred clinical research partner - Collaborate with and provide oversight of deliverables from vendors locally, if applicable - Support the site in filing and archiving trial documentation in the Investigator Trial Master File (ITMF) - Participate in Investigators Meetings to ensure relations with sites as well as active presentation as applicable - Maintain knowledge of and act in compliance with global and local SOPs, GCP and other regulatory requirements - Support audits and inspections at sites and affiliate, as applicable Número de vacantes: 1 Modalidad de trabajo: Full remoto (100%) Tipo de contrato: Indefinido **Ventajas sociales o económicas** Competitive salary and additional social benefits (Health Insurance, Life Insurance, Lunch vouchers) " **Requisitos** - Bachelor or Master’s degree in life sciences or other relevant fields. - At least 1-2 years of experience as a Clinical Research Associate. - Therapeutic area knowledge and demonstrating an understanding of oncology (solid tumors) phase I studies is an advantage. - Excellent knowledge of Clinical Trial Management Systems, Good -Clinical Practices and Trial Management. - Strong analytical and communication skills with business, industry understanding and stakeholder management. - Fluent in both Portuguese and English. - Valid driver’s license. Estudios mínimos Licenciado **Idiomas**: Inglés nível Perfecto. - Experiência mínima 2 años Disponibilidad para viajar El 40% del tiempo laboral
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Clinical Research Associate Ii
Há 22 horas
Porto, Portugal IQVIA LLC Tempo inteiroSenior Clinical Research Associate - based in Portugal page is loaded## Senior Clinical Research Associate - based in Portugallocations: Porto Salvo, Portugaltime type: Full timeposted on: Posted Todayjob requisition id: R1482219Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study...
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Experienced Clinical Research Associate
Há 2 dias
Porto Salvo, Portugal IQVIA Tempo inteiroSenior Clinical Research Associate Your responsibilities will include: Performing site selection, initiation, monitoring and close-out visits Supporting the development of a subject recruitment plan Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on...
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Clinical Research Associate II
1 semana atrás
Porto, Portugal PSI CRO Tempo inteiroCompany Description PSI is a leading Contract Research Organization with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we...
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Clinical Research Associate II
Há 7 dias
Porto, Porto, Portugal PSI CRO Tempo inteiroCompany Description PSI is a leading Contract Research Organization with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we...
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Experienced Clinical Research Associate
Há 3 dias
Porto Salvo, Lisboa, Portugal IQVIA Tempo inteiroSenior Clinical Research Associate Your responsibilities will include:Performing site selection, initiation, monitoring and close-out visitsSupporting the development of a subject recruitment planEvaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on...
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Experienced Clinical Research Associate
Há 6 dias
Porto, Portugal IQVIA LLC Tempo inteiroSenior Clinical Research Associate - based in Portugal page is loaded## Senior Clinical Research Associate - based in Portugallocations: Porto Salvo, Portugaltime type: Full timeposted on: Posted Todayjob requisition id: R1482219Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting...
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Experienced Clinical Research Associate
Há 6 dias
Porto Salvo, Portugal IQVIA Tempo inteiroSenior Clinical Research Associate Your responsibilities will include:Performing site selection, initiation, monitoring and close-out visitsSupporting the development of a subject recruitment planEvaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on...
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Project Management Associate
1 semana atrás
Porto, Portugal TFS HealthScience Tempo inteiroTFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions.Join Our Team as a Project Management Associate - (home...
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Project Management Associate
2 semanas atrás
Porto, Porto, Portugal TFS HealthScience Tempo inteiroTFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions.Join Our Team as a Project Management Associate - (home...
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Sr/ Clinical Trial Manager
2 semanas atrás
Porto Salvo, Portugal IQVIA Tempo inteiroClinical Trial Manager - IQVIA Biotech * Please note: due to sponsor requirements for the role only candidates based in the listed location/s and with previous Global CTM experience will be considered. Any applications from candidates based outside of these locations will not be considered.Job Overview Clinical Trial Managers (CTM) are an integral part of...
