Lavori attuali relativi a Clinical Trial Associate - Bardi - Planet Pharma
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Bardi, Italia Icon A tempo pienoA leading clinical research organization is seeking a Clinical Research Associate II to play a crucial role in clinical trial design and analysis. This home-based position requires a Bachelor's degree and at least 2 years of CRA experience, with a solid understanding of clinical trial processes. The role involves extensive traveling and offers competitive...
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Senior Clinical Trial Manager
7 ore fa
Bardi, Italia Syneos Health, Inc. A tempo pienoA leading biopharmaceutical solutions organization is looking for a Sr.Clinical Trial Manager (Clinical Research Medical Advisor) to provide medical and scientific leadership for clinical trials in Italy.In this homebased role, you will lead trial implementation, support regulatory interactions, and ensure compliance with standards.The ideal candidate has a...
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Freelance Clinical Project Manager
6 giorni fa
Bardi, Italia Epm Scientific A tempo pienoEPM Scientific are currently partnered with a Biotechnology company who are seeking a Freelance Clinical Project Manager to support their Rare Disease trials in Italy.See a short summary below: Contract Conditions: Start date: ASAP Location: Italy Contract: 0.8 - 1 FTE, 12-Month Contract Project: Rare Neuromusclar Disease - Phase 2 Trial Key Responsibilities...
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Experienced Clinical Research Associate, Iqvia Biotech
2 settimane fa
Bardi, Italia Wolters Kluwer A tempo pienoExperienced Clinical Research Associate, IQVIA Biotech - Home based, ItalyTheForkRemotoEUR ***************3 giorni faPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.Essential...
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Freelance Clinical Project Manager
6 giorni fa
Bardi, Italia Epm Scientific A tempo pienoEPM Scientific are currently partnered with a Biotechnology company who are seeking a Freelance Clinical Project Manager to support their Rare Disease trials in Italy.See a short summary below:Contract Conditions:Start date: ASAPLocation: ItalyContract: 0.8 - 1 FTE, 12-Month ContractProject: Rare Neuromusclar Disease - Phase 2 TrialKey ResponsibilitiesLead...
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Clinical Specialist Biosurgery
2 settimane fa
Bardi, Italia Bd Nogales Norte A tempo pienoClinical Specialist Biosurgery & Infection Prevention Join to apply for the Clinical Specialist Biosurgery & Infection Prevention role at BD Nogales NorteThe Clinical Specialist role involves providing comprehensive clinical and technical support to the sales team and customers across Italy for BIP solutions, including training, operating room activities,...
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Cra Ii/Senior Cra
1 minuto fa
Bardi, Italia Icon A tempo pienoOverview CRA II, Senior CRA home based Poland 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 Clinical Research...
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Global Clinical Project Manager
2 settimane fa
Bardi, Italia Iqvia A tempo pieno?Please note that, due to specific sponsor's requests, we can only consider candidates with minimum one year of prior Global LEAD experience and coming from the locations where the job advertisement is posted.Applications from other locations will not be considered.*Job OverviewProject Leads are an integral part of clinical trial delivery, liaising with...
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Clinical Research Associate
22 ore fa
Bardi, Italia Opis A tempo pienoLocalitàProvince of Monza and Brianza, ItalyAziendaOPIS - Guarda altre offerteLocalitàProvince of Monza and Brianza, ItalyDescrizioneParticipate in the feasibility process of new studies/clinical investigations, collect feasibility questionnaire (if applicable) and other documents necessary for the ethical and administrative (...)Perform...
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Clinical Research Associate
23 ore fa
Bardi, Italia Opis A tempo pienoLocalitàProvince of Monza and Brianza, ItalyAziendaOPIS - Guarda altre offerteLocalitàProvince of Monza and Brianza, ItalyDescrizioneParticipate in the feasibility process of new studies/clinical investigations, collect feasibility questionnaire (if applicable) and other documents necessary for the ethical and administrative [...]Perform...
Clinical Trial Associate
3 ore fa
Planet Pharma is seeking a Clinical Trial Associate (CTA) to provide key operational and administrative support to a global Clinical team.This role plays an important part in maintaining quality systems, training compliance, documentation and clinical platforms, helping to ensure efficient and compliant clinical development activities.Key ResponsibilitiesMaintain and regularly update SOP inventories, training matrices and compliance documentation.Coordinate, assign, track and document training activities in line with regulatory and internal requirements.Support clinical administrative processes including CV management, onboarding documentation, vendor tracking and organizational charts.Manage system access and user coordination for platforms such as eTMF, Veeva QDocs and DocuSign, working closely with IT and internal stakeholders.Assist with the planning and coordination of internal and external meetings, ensuring logistics, materials and documentation are prepared.Serve as first-line support for basic system and access-related issues, ensuring clear and effective communication with relevant teams.Qualifications & SkillsBachelor's degree in a scientific, pharmaceutical, biomedical or related discipline (or equivalent relevant experience).Strong working knowledge of Microsoft Office (Excel, Word, PowerPoint, Outlook and SharePoint).Highly organized with strong attention to detail and the ability to manage multiple priorities in a fast-paced environment.Fluency in English (written and spoken) is required.Fluency in Italian is required.Preferred experience within clinical research, pharmaceutical, or biotech environments, with familiarity in systems such as SAP SuccessFactors, eTMF, DocuSign and Veeva QDocs and an understanding of 21 CFR Part 11.#J-*****-Ljbffr
