Senior Cra

hace 3 meses


Madrid, España Icon Strategic Solutions A tiempo completo

.As a Clinical Research Associate (CRA) you will coordinate all aspects of the clinical monitoring and site management process in accordance with regulatory guidelines, local regulations and standard operating procedures. In this role you will be a decision maker, solving problems independently or as part of the client and ICON team.You will be managing competing priorities, supporting the on-site team, ensuring investigators follow the clinical trial protocol, providing training, and most importantly, motivating the team to ensure high quality results.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: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.Why ICON?Our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.Our success depends on the knowledge, capabilities and quality of our people


  • Cra Andalucia

    hace 5 meses


    Madrid, España TFS HealthScience A tiempo completo

    Overview: CLINICAL RESEARCH ASSOCIATE ANDALUCÍA - SINGLE SPONSOR TFS HealthScience is excited to be expanding our SRS** **team and we are looking for an experienced, highly motivated regional Senior Clinical Research Associate (CRA) who shares our vision of providing clinical research excellence. Our SRS team is a highly experienced international group of...

  • Senior Cra

    hace 3 semanas


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    .As a Clinical Research Associate (CRA), you will coordinate all aspects of the clinical monitoring and site management process in accordance with regulatory guidelines, local regulations, and standard operating procedures. In this role, you will be a decision maker, solving problems independently or as part of the client and ICON team.You will manage...

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    hace 1 mes


    Madrid, España Mygwork A tiempo completo

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  • Senior Cra

    hace 2 meses


    Madrid, España Icon A tiempo completo

    .As a Clinical Research Associate (CRA), you will coordinate all aspects of the clinical monitoring and site management process in accordance with regulatory guidelines, local regulations, and standard operating procedures. In this role, you will be a decision maker, solving problems independently or as part of the client and ICON team.You will be managing...

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    hace 1 mes


    Madrid, España Pharmiweb A tiempo completo

    Senior CRA - Spain, Madrid ICON plc is a world-leading healthcare intelligence and clinical research organization.We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.We are currently seeking a Senior Clinical Research Associate to join our...

  • Cra

    hace 1 mes


    Madrid, España Mygwork A tiempo completo

    This job is with ICON plc, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community.Please do not contact the recruiter directly.Senior CRA - Spain, Madrid ICON plc is a world-leading healthcare intelligence and clinical research organization.We're proud to foster an inclusive environment driving...

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    hace 1 semana


    Madrid, España Mygwork A tiempo completo

    This job is with ICON plc, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community.Please do not contact the recruiter directly.Senior CRA - Spain, Madrid ICON plc is a world-leading healthcare intelligence and clinical research organization.We're proud to foster an inclusive environment driving...

  • Senior Cra

    hace 3 semanas


    Madrid, España Engineeringuk A tiempo completo

    As a Clinical Research Associate (CRA), you will coordinate all aspects of the clinical monitoring and site management process in accordance with regulatory guidelines, local regulations, and standard operating procedures. In this role, you will be a decision maker, solving problems independently or as part of the client and ICON team.You will manage...

  • Cra

    hace 1 semana


    Madrid, España Mygwork A tiempo completo

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    As a Clinical Research Associate (CRA) you will coordinate all aspects of the clinical monitoring and site management process in accordance with regulatory guidelines, local regulations and standard operating procedures. In this role you will be a decision maker, solving problems independently or as part of the client and ICON team. You will be managing...


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    Job SummaryWe are seeking a highly skilled and experienced Senior Clinical Operations Manager to lead our CRA team. As a key member of our Clinical Operations Management Team, you will be responsible for managing and motivating a team of Clinical Research Associates (CRAs) to deliver high-quality services.Key ResponsibilitiesDevelop and implement action...

  • Sr Cra

    hace 5 meses


    Madrid, España Novasyte A tiempo completo

    Internal Job Description - Join us in our exciting journey!!- We currently require a motivated, creative and enthusiastic clinical trials professional to join our rapidly growing Site Management division.- As an experienced Clinical Research Associate, you could be looking to broaden your therapeutic, geographic or study exposure. Or perhaps you are looking...


  • Madrid, Madrid, España Tfs Healthscience A tiempo completo

    About the RoleWe are seeking a highly skilled Senior Clinical Research Associate to join our team at Tfs Healthscience. As a key member of our SRS/FSP team, you will be dedicated to a global biotech company that is an industry leader in onco-hematology.Key ResponsibilitiesMonitor clinical trials in accordance with Tfs and/or client company Standard Operating...


  • Madrid, Madrid, España Tfs Healthscience A tiempo completo

    About the RoleWe are seeking a highly skilled Senior Clinical Research Associate to join our team at Tfs Healthscience. As a key member of our SRS/FSP team, you will be dedicated to a global biotech company that is an industry leader in onco-hematology.Key ResponsibilitiesMonitor clinical trials in accordance with Tfs and/or client company Standard Operating...

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    hace 5 meses


    Madrid, España ICON plc A tiempo completo

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    This role with ICON plc, an inclusive employer and a member of the LGBTQ+ business community, involves coordinating clinical monitoring and site management processes in accordance with regulatory guidelines and standard operating procedures.As a Clinical Research Associate, you will be a decision-maker, solving problems independently or as part of the client...


  • Madrid, Madrid, España Mygwork A tiempo completo

    This role is with ICON plc, an inclusive employer and a member of the LGBTQ+ business community.As a Clinical Research Associate (CRA), you will coordinate all aspects of the clinical monitoring and site management process in accordance with regulatory guidelines, local regulations, and standard operating procedures.In this position, you will be a decision...


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