Lavori attuali relativi a Clinical Research Associate - Florence - Translational Oncology Research, LLC
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Clinical Research Associate
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Florence, Italia TRIO - Translational Research in Oncology A tempo pienoOverviewTRIO is looking for a Clinical Research Associate to join our Monitoring Resources team. Reporting to a CRA Line Manager, this position will be home-based in Italy.Translational Research in Oncology (TRIO) is a global clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team...
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Senior Clinical Research Associate
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Florence, Italia Ascom UMS A tempo pienoA leading company in the Pharma Sector located in Florence, Italy, is seeking a Senior Clinical Research Associate. In this role, you will ensure compliance with SOPs and conduct site monitoring visits while managing data accuracy and adverse event reporting. Ideal candidates will have at least 10 years of relevant experience, including exposure to ATTR...
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Senior Clinical Research Associate
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Florence, Italia Red Bull Gruppe A tempo pienoA leading pharmaceutical company in Florence is seeking a Senior Clinical Research Associate to ensure compliance with regulations and support site teams. The ideal candidate will have over 10 years of experience, ideally in ATTR cardiac amyloidosis or non-interventional studies. This role involves site initiation, monitoring, data accuracy, and supporting...
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Clinical research associate
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Florence, Italia Hays A tempo pienoYour new companyOur client is a leading company in the Pharma Sector.We are seeking a Senior Clinical Research Associate to join our teamYou new roleEnsure compliance with client SOPs, study protocols, ICH-GCP and applicable regulationsTrain and support investigator site teams on study procedures and systemsConduct site initiation, monitoring (on-site and...
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Bayesian Clinical Trials Postdoc
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Florence, Italia ManpowerGroup A tempo pienoA leading research institution is seeking a Postdoc for a project focused on Bayesian Methods for Clinical Studies. This position offers a salary of EUR 30,000 - 38,000, remote work options, and a duration of 16 months. Candidates must have a Ph.D. and a non-Italian affiliation for at least 24 months in the past three years. Interested applicants should send...
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Informatore scientifico veterinario
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Advanced Practice Provider
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Informatore scientifico veterinario
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Florence, Italia Grafton Recruitment A tempo pienoGrafton LifeScience è la specializzazione di Gi Group dedicata a valorizzare le esperienze, le competenze e il potenziale dei candidati in ambito Sales&Marketing, Clinical Research, Regulatory e Operation dei settori Farmaceutico e Medicale e per le mansioni legate all’assistenza al cliente del mondo distributivo con impatto sulla salute. Il nostro...
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Informatore scientifico veterinario
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Florence, Italia Grafton Recruitment A tempo pienoGrafton LifeScience è la specializzazione di Gi Group dedicata a valorizzare le esperienze, le competenze e il potenziale dei candidati in ambito Sales&Marketing, Clinical Research, Regulatory e Operation dei settori Farmaceutico e Medicale e per le mansioni legate all’assistenza al cliente del mondo distributivo con impatto sulla salute. Il nostro...
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Informatore scientifico veterinario
3 settimane fa
Florence, Italia Grafton Recruitment A tempo pienoGrafton LifeScience è la specializzazione di Gi Group dedicata a valorizzare le esperienze, le competenze e il potenziale dei candidati in ambito Sales&Marketing, Clinical Research, Regulatory e Operation dei settori Farmaceutico e Medicale e per le mansioni legate all’assistenza al cliente del mondo distributivo con impatto sulla salute. Il nostro...
Clinical Research Associate
3 ore fa
OverviewTranslational Research in Oncology (TRIO) is a global clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing cancer treatments of the future to the world of today. TRIO is looking for a Clinical Research Associate to join our Monitoring Resources team. Reporting to a CRA Line Manager, this position will be home-based in Italy.ResponsibilitiesConducting site visits, including pre-study, initiation, monitoring, and terminationConfirming adherence to all FDA, ICH-GCP and local regulationsEnsuring the completion and collection of regulatory documentsPerforming data verification of source documentsEnsuring implementation and compliance with FDA, ICH-GCP guidelinesParticipating in budget negotiation and follow-up where applicableAssisting with data validation and query resolutionMentoring junior team members as requiredQualificationsA minimum of 2 years of monitoring experience in oncology trialsExperience in monitoring early-phase trialsFluent in EnglishCompletion of a science-related Bachelor’s degreeExcellent knowledge of medical terminology and clinical monitoring processStrong ICH-GCPs knowledgeExperience with clinical trial information systemsAbility to travel up to 60% on averageWhat TRIO Can Offer YouCompetitive salaryPaid annual leaveHealth insurance planFlexible working hoursLuggage allowanceMobile phone allowanceSalary to be influenced (or determined) by the education, experience, location, knowledge, skills, abilities of the applicant, internal equity, and alignment with market data.If you are interested, please submit your resume in English. We thank all candidates for their interest; only those selected for an interview will be contacted.Prior to applying please review TRIO's Applicant Information Notice.To support efficiency, TRIO may use limited AI tools during the candidate review process. All hiring decisions are made by people, not AI.TeamworkPassionIntegrityInnovationPowered by JazzHR#J-18808-Ljbffr
