icf

A INVESCORTE - Computadores e sistemas, S.A. está a recrutar um vendedor para impulsionar o crescimento comercial das suas soluções CAD/CAM e ICF na indústria do vestuário e industrial. Procuramos alguém que domine todo o ciclo de vendas, desde a prospeção até ao fechamento.Oferecemos um salário base competitivo entre €****** e €******/ano, uma...

A Invescorte - Computadores E Sistemas procura um(a) Vendedor(a) comissionado(a) para expandir as vendas de soluções CAD/CAM e ICF na indústria têxtil e industrial em Viseu. O candidato deve dominar o ciclo de vendas e a prospecção de novos clientes. É valorizada a capacidade de estruturar abordagens comerciais, manter relacionamentos com clientes e...

CTI Clinical Trial And Consulting Services in Portugal seeks a Regulatory Affairs professional to lead start-up strategies for European trials, coordinate submissions, and ensure country-specific compliance.You will collaborate with sponsors, sites, and IRBs, adapt ICFs, prepare regulatory dossiers, and maintain TMF quality, with English fluency required.A...

What You'll Do: Regulatory Submission Management • Prepare, review, and manage regulatory submissions under CTR (Clinical Trials Regulation) using CTIS. • Handle regulatory submissions for medical devices, GMOs, and local country requirements in countries where CTIS is not mandated, including ethics committee submissions. • Prepare and QC Clinical...

Principal RASSU Specialist Empresa : Join The Cti Team Tipo de Emprego : Periodo Integral Portugal Descrição do Emprego - Principal RASSU Specialist ** Please submit your application in English ** WhatYou'llDo: - Assist/Advise project teams on all regulatory requirements for clinical studies - Perform compliance assessments according to country...

CTI Clinical Trial And Consulting Services in Portugal seeks a Regulatory Affairs professional to lead start-up strategies for European trials, coordinate submissions, and ensure country-specific compliance. You will collaborate with sponsors, sites, and IRBs, adapt ICFs, prepare regulatory dossiers, and maintain TMF quality, with English fluency required. A...

** Please submit your application in English ** What You'll Do: Support of Regulatory Affairs Study Start-Up (RASSU) department: - Assist/Advise project teams on all regulatory requirements for clinical studies - Perform compliance assessments according to country requirements and document any activity discovered; notify Project Managers of any findings -...

Principal RASSU Specialist Empresa : Join The Cti Team Tipo de Emprego : Periodo Integral Portugal Descrição do Emprego - Principal RASSU Specialist ** Please submit your application in English ** WhatYou'llDo: Assist/Advise project teams on all regulatory requirements for clinical studies Perform compliance assessments according to country...

What You'll Do: Regulatory Submission Management Prepare, review, and manage regulatory submissions under CTR (Clinical Trials Regulation) using CTIS. Handle regulatory submissions for medical devices, GMOs, and local country requirements in countries where CTIS is not mandated, including ethics committee submissions. Prepare and QC Clinical Trial...

Principal RASSU Specialist Empresa : Join The Cti Team Tipo de Emprego : Periodo Integral Portugal Descrição do Emprego - Principal RASSU Specialist ** Please submit your application in English ** WhatYou'llDo: Assist/Advise project teams on all regulatory requirements for clinical studies Perform compliance assessments according to country...

** Please submit your application in English ** What You'll Do: Support of Regulatory Affairs Study Start-Up (RASSU) department: Assist/Advise project teams on all regulatory requirements for clinical studies Perform compliance assessments according to country requirements and document any activity discovered; notify Project Managers of any findings Review...

** Please submit your application in English ** What You'll Do: Support of Regulatory Affairs Study Start-Up (RASSU) department: Assist/Advise project teams on all regulatory requirements for clinical studies Perform compliance assessments according to country requirements and document any activity discovered; notify Project Managers of any findings Review...

Descrição do cargo What You/'ll Do - Assist/Advise project teams on all regulatory requirements for clinical studies - Perform compliance assessments according to country requirements and document any activity discovered; notify Project Managersof any findings - Review and adapt study specific documents according each country and site requirements -...

Join us as a Behavioral Health Coach on our innovative telehealth platform, Intellect, where you'll empower clients to enhance their mental well-being and achieve personal growth. Using your expertise, you'll guide clients through personalized, 30-minute video sessions designed around their unique goals. This flexible freelance role allows you to set your...

A CTI, empresa global de pesquisa clínica, procura um Principal RASSU Specialist para liderar atividades regulatórias em estudos clínicos em Portugal. O candidato ideal tem sólida experiência em conformidade regulatória, preferencialmente em CROs, e domínio de requisitos de IRB/EC locais. Principais funções: assessorar equipas, preparar e submeter...

Acorai is a Swedish medtech company building the SAVE Sensor System — a non-invasive, handheld device that estimates intracardiac filling pressures at the bedside. Today the only reliable way to measure those pressures is right heart catheterisation: invasive, expensive, and confined to a cath lab. We are replacing it with a short bedside recording. Heart...

** Please submit your application in English ** What You'll Do: Support of Regulatory Affairs Study Start-Up (RASSU) department: Assist/Advise project teams on all regulatory requirements for clinical studies Perform compliance assessments according to country requirements and document any activity discovered; notify Project Managers of any findings Review...

Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. Job Overview Perform tasks at a country level...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the...