Empregos de icf em Lisboa

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...

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...

The Site Navigator Intern supports site-level activities throughout study start-up and, maintenance and closeout.Under the guidance of experienced team members, the intern assists with feasibility, site outreach, site activation, regulatory compliance, and site support, while gaining practical experience in clinical research operations and cross-functional...

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...

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...

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. Opportunity within FSP for a Regulatory and Start Up...

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...

Reading, Berkshire, United KingdomZagreb, CroatiaLisbon, PortugalBarcelona, SpainPrague, Czech RepublicMadrid, SpainFull timeR*******The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client's project team in the execution of clinical trials.Joining the team provides the opportunity to manage...

Descrição do cargoWhat You\ 'll DoAssist/Adviseproject teams on all regulatory requirements for clinical studiesPerform compliance assessments according to country requirements and document any activity discovered;Notify Project Managersof any findingsReview and adapt study specific documents according each country and site requirementsPerform IRB/EC (CA)...

SAP BTP Lead - English speaking - Portugal (Lisbon or 100% Remote from within Portugal).Permanent Job.Start: Q****** +/-.Salary: Up to €75,000/annum plus Benefits.Our client is looking for an SAP BTP (SAP Business Technology Platform) Lead as part of the SAP Technical and Transformation Practice.As a key player in transformation, the SAP BTP Technical...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAt 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 resources needed to...

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 Managersof 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 studiesPerform compliance assessments according to country requirements and document any activity discovered; notify Project Managersof any findingsReview and...

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...

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...

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...

The Site Navigator Intern supports site-level activities throughout study start-up and, maintenance and closeout. Under the guidance of experienced team members, the intern assists with feasibility, site outreach, site activation, regulatory compliance, and site support, while gaining practical experience in clinical research operations and cross-functional...

Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job DescriptionJoin Us as an Associate Medical Director – Make an Impact at the Forefront of Innovation 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...

** 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 Managersof any findings Review and...