Empregos actuais relacionados com Clinical Research Associate - Lisboa - ICON
-
Clinical Research Associate
2 semanas atrás
Lisboa, Portugal TFS HealthScience Tempo inteiroOverview: TFS HealthScience is excited to be expanding our Site Management team and we are looking for an experienced, highly motivated Clinical Research Associate (CRA) who shares our vision of providing clinical research excellence. Our Site Management team is a highly experienced international group of professionals led by an industry expert. We are a...
-
Senior Clinical Research Associate
Há 5 horas
Lisboa, Portugal TFS HealthScience Tempo inteiroTFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions. **Join Our Team as a** **Senior Clinical Research...
-
Clinical Research Associate II
1 semana atrás
Lisboa, Lisboa, Portugal PSI CRO Tempo inteiroCompany Description PSI is a leading Contract Research Organization with almost 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Job Description As a Clinical Research Associate II at PSI you...
-
Freelance Clinical Research Associate
Há 7 dias
Lisboa, Portugal EPM Scientific Tempo inteiroEPM Scientific are currently partnered with a Mid-Sized CRO running a global project in Oncology. They are urgently seeking a Freelance Clinical Research Associate (CRA) to support their expanding clinical operations team. See a short summary below: **Contract Conditions**: - Start date: ASAP - Location: Portugal, Remote - Contract Type: Freelance /...
-
Clinical Research Associate 2
1 semana atrás
Lisboa, Lisboa, Portugal IQVIA Tempo inteiroClinical Research Associate Your 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...
-
Clinical Research Associate, Full-service
Há 5 horas
Lisboa, Portugal Novasyte Tempo inteiroJoin us in our exciting journey!! As an experienced Clinical Research Associate, you could be looking to broaden your therapeutic, geographic or study exposure. Or perhaps you are looking a future beyond monitoring with our selection of development opportunities. At IQVIA, you’ll have training and development to plan and progress your career in the...
-
Clinical Trial Associate
Há 5 horas
Lisboa, Portugal TFS HealthScience Tempo inteiroTFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions. **Join Our Team as a Clinical Trial Associate...
-
Clinical Research Associate I
Há 5 dias
Lisboa, 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. With over 19,000 staff...
-
Clinical Trial Associate
Há 5 horas
Lisboa, Portugal TFS HealthScience Tempo inteiroOverview: TFS HealthScience is excited to be expanding our **SRS** team and we are looking for an experienced, highly motivated **CLINICAL TRIAL ASSOCIATE** who shares our vision of providing clinical research excellence. Our **SRS **team is a highly experienced international group of professionals led by an industry expert. We are a leading global...
-
Clinical Trial Assistant 2
Há 5 horas
Lisboa, Portugal Novasyte Tempo inteiroClinical Trial Administrator, Single Sponsor dedicated Job Overview: CTA performs daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. By assisting in the coordination and administration of the study activities from the start up...
Clinical Research Associate
3 semanas atrás
As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. **What you will be doing**: - You will monitor multiple Phase I, II, III & IV clinical trial sites, across different therapeutic areas. Assist other CRAs with co-monitoring activities both remote and on-site. - You will utilise your customer service mindset with your sites focusing on delivering value, building loyalty and trust to create a positive impact and strong relationship with investigators and study coordinators where respect, knowledge and commitment to ICH/GCP guidelines are key to successful trial conduct. - As the CRA you are the main sponsor representative, providing key project updates. You will collaborate with the team, developing commitment to study timelines and objectives through regular visits with site staff in-person and remotely. - You will be first to review "source to CRF/eCRF," ensuring patient safety and data integrity aspect of the study. - As the first point of contact for study sites, escalating any concerns/issues to other departments including Safety, Investigational Medicinal Product, Local Study Managers and management team as appropriate. - Additionally, you will oversee the sites' adherence to GCP/ICH practices, ensuring quality of study conduct. **You are**: - Based in Lisbon area - Bachelor’s Degree (or equivalent) with 2-4 years of relevant healthcare experience in the pharma or clinical research industry. Minimum 6-12 months of monitoring and site management experience - Scientific background - Proficiency with medical terminology - Working knowledge of Local Regulations - A demonstrated working knowledge of ICH/GCP Guidelines - Excellent record-keeping skills and attention to detail - Experience conducting Site Selection, Initiation, Routine Monitoring and Close Out Visits both remotely and on-site - Fluent in English, both written and oral - Strong technical skills with CTMS, eCRF, eTMF **What ICON can offer you**: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: - Various annual leave entitlements - A range of health insurance offerings to suit you and your family’s needs - Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead - Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being - Life assurance - Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others
