Experienced Clinical Research Associate
2 semanas atrás
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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Senior Clinical Research Associate
2 semanas atrás
Oeiras, Lisboa, Portugal MSD Portugal Tempo inteiro 60 000 € - 120 000 € por anoJob DescriptionWe are one of the leading pharmaceutical companies in the world, dedicated to the discovery, development, and delivery of innovative medicines that improve health and quality of life for people. With a strong global presence and an unwavering commitment to scientific research, our mission is to transform health through innovation and...
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Senior Clinical Research Associate
2 semanas atrás
Oeiras, Lisboa, Portugal MSD Tempo inteiro 40 000 € - 80 000 € por anoJob DescriptionWe are one of the leading pharmaceutical companies in the world, dedicated to the discovery, development, and delivery of innovative medicines that improve health and quality of life for people. With a strong global presence and an unwavering commitment to scientific research, our mission is to transform health through innovation and...
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Clinical Research Associate
2 semanas atrás
Oeiras, Portugal IQVIA Tempo inteiroClinical Research Associate - based in Porto 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...
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Senior Clinical Research Associate
7 minutos atrás
Oeiras, Portugal Fortrea Tempo inteiro**Senior Clinical Research Associate (SRCRA )** **Job Overview** Join Fortrea as a SR Clinical Research Associate - Drive Clinical Excellence in Cardiovascular and 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...
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Clinical Research Associate 2
1 semana atrás
Oeiras, Portugal IQVIA Tempo inteiroClinical 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 2
Há 3 dias
Oeiras, Portugal IQVIA Tempo inteiroClinical 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 2
2 semanas atrás
Oeiras, Lisboa, Portugal IQVIA Tempo inteiro 40 000 € - 60 000 € por anoClinical 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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Oeiras, Lisboa, Portugal IQVIA Tempo inteiroClinical 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
4 semanas atrás
Oeiras, Portugal IQVIA Tempo inteiroClinical 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...
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Clinical Research Associate Ii
2 semanas atrás
Oeiras, Portugal Fortrea Tempo inteiroAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in...
