Desculpe, a oferta não está disponível,
mas você pode realizar uma nova pesquisa ou explorar ofertas semelhantes:

Open Call For A Post-Doctoral Fellowship

OPEN CALL FOR A POST-DOCTORAL FELLOWSHIP2-year post-doctoral research position funded by the EU H2020 Project RELOCAL "Resituating the Local in Cohesion and ...


University Of Groningen - Lisboa

Publicado a month ago

Medische Producten Adviseur (Nederlands)

.Ben je geïnteresseerd in geneeskunde? En wil je graag mensen met een ziekte helpen? Werk voor een bedrijf in medische hulpmiddelen dat het leven van mensen ...


Blu Selection - Lisboa

Publicado a month ago

Data Driven | Data Scientist

At Devoteam, we believe that technology with strong human values can actively drive change for the better. Discover how Tech for People unlocks the future, c...


Devoteam - Lisboa

Publicado a month ago

Técnico De Laboratório E Garantia De Qualidade - Peniche

Técnico de Laboratório e Garantia de Qualidade - Peniche  (m/f)Referencia: JN -******** Adicionado em 11.10.2024 Sobre os nossos clientes O nosso cliente...


Michael Page Portugal - Lisboa

Publicado a month ago

Senior Clinical Research Associate - Sponsor Dedicated- Based In Portugal

Detalhes da Vaga

IQVIA is the Human Data Science Company oriented to drive human health outcomes forward. When you join IQVIA Portugal as a sponsor-dedicated CRA, you'll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our customers. With access to world-class training and mentoring, you'll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas. 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 (GCP) and International Conference on Harmonization (ICH) guidelines Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution Collaborating with experts at study sites and with client representatives Qualifications: University degree in scientific discipline or health care At least 2 years of on-site monitoring experience Good knowledge of clinical research regulatory requirements 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 Better Work-Life balance, optimal DOS Excellent working environment in a stabile, international, reputable company Company car, mobile phone and attractive benefits package #LI-DARIASHV #CRASDAJD IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at #J-18808-Ljbffr


Salário Nominal: A acordar

Fonte: Jobtome_Ppc

Função de trabalho:

Requisitos

Built at: 2024-11-09T22:59:34.152Z