Experienced Clinical Research Associate
Há 7 dias
Senior 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 Harmonization guidelines Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutionsCollaborating with experts at study sites and with client representatives Qualifications: University degree in scientific discipline or health care Requires at least 3 year of on-site monitoring experience. Very good computer skills including MS Office Excellent command of Portuguese and English language. Organizational, time management and problem-solving skills Ability to establish and maintain effective working relationships with coworkers, managers, and clients Flexibility to travel Driver's license class B What you can expect: Resources that promote your career growth Leaders that support flexible work schedules Programs to help you build your therapeutic knowledge Excellent working environment in a stabile, international, reputable company Company car, mobile phone and attractive benefits package IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at . At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes.
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Experienced Clinical Research Associate
2 semanas atrás
Oeiras, Portugal IQVIA Tempo inteiroClinical Research Associate needed in Porto to perform site visits and support recruitment plans.
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Experienced Clinical Research Associate
2 semanas atrás
Oeiras, 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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Experienced Clinical Research Associate
2 semanas atrás
Oeiras, Lisboa, Portugal IQVIA Tempo inteiroSenior Clinical Research AssociateYour 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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Clinical Research Associate 2
Há 18 horas
Oeiras, Portugal Fortrea Tempo inteiroA global clinical research organization seeks a Clinical Research Associate 2 in Portugal. Responsibilities include site monitoring, ensuring patient safety, and compliance with regulatory guidelines in clinical studies. The ideal candidate should have a degree in a health-related field, at least one year of CRA experience, and strong English communication...
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Clinical Research Assoicate
2 semanas atrás
Oeiras, Portugal IQVIA Tempo inteiroJob Description We are seeking a highly skilled Clinical Research Associate (CRA) to lead performance and compliance for assigned protocols and sites within Portugal - Zona Norte . Under the oversight of the CRA Manager, you will serve as the primary site contact throughout all phases of clinical studies, ensuring rigorous adherence to ICH/GCP, local...
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Clinical Research Associate 2
2 semanas atrás
Oeiras, Portugal Fortrea Tempo inteiroClinical Research Associate 2 - FSO Model - Portugal Join to apply for the Clinical Research Associate 2 - FSO Model - Portugal role at Fortrea. Job Overview Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Ensures the implementation of...
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Senior Clinical Research Associate
Há 3 dias
Oeiras, Portugal Fortrea Tempo inteiroJoin Fortrea as a SR Clinical Research Associate - Drive Clinical Excellence in Oncology Trials. This role is for upcoming future opportunities that may arise at Fortrea. As a SRCRA, you will ensure clinical studies are conducted to the highest regulatory and quality standards, protecting patient safety and delivering reliable data. You’ll coordinate...
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Porto-Based Clinical Research Associate
1 semana atrás
Oeiras, Portugal Phiture Tempo inteiroA clinical research organization is seeking a Clinical Research Associate (CRA) to lead performance and compliance for assigned protocols. You will manage site activities across Portugal, ensuring adherence to regulations and quality standards. The role requires a Bachelor’s degree and a minimum of 3 years direct site management experience in the...
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Clinical Research Assoicate
2 semanas atrás
Oeiras, Portugal MSD Tempo inteiroJob Description We are seeking a highly skilled Clinical Research Associate (CRA) to lead performance and compliance for assigned protocols and sites within Portugal - Zona Norte . Under the oversight of the CRA Manager, you will serve as the primary site contact throughout all phases of clinical studies, ensuring rigorous adherence to ICH/GCP, local...
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Clinical Research Assoicate
2 semanas atrás
Oeiras, Portugal MSD Portugal Tempo inteiroJob DescriptionWe are seeking a highly skilledClinical Research Associate (CRA)to lead performance and compliance for assigned protocols and sites withinPortugal - Zona Norte. Under the oversight of the CRA Manager, you will serve as the primary site contact throughout all phases of clinical studies, ensuring rigorous adherence to ICH/GCP, local regulations,...
