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Dettagli di lavoro

Riepilogo

    Pubblicato il 17. febbraio 2026

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    Dettagli di lavoro

    Position Snapshot


    Location: Vers-chez-les-Blanc, Switzerland

    Entity: Clinical Research Unit, Nestlé Research

    Work rate: 100%

    Contract type: Temporary

    Duration: 12 months

    ...

    Summary

    The Senior Clinical Trial Assistant (Sr. CTA) provides high-quality operational and administrative support to clinical trial teams throughout all phases of a pharmaceutical study. Operating within a fast-paced, regulated environment, the Sr. CTA ensures clinical documentation is accurately maintained, processes are followed, and systems are updated in a timely and compliant manner. This position works cross-functionally with internal stakeholders and external partners (e.g., CROs, vendors, investigator sites) to enable successful study execution in line with relevant pharmaceutical standards.



    Responsibilities

    • Support the Clinical Project Manager(s) in study execution, including tracking study milestones and key deliverables
    • Maintain and manage the Trial Master File (TMF/eTMF), performing periodic completeness and quality reviews
    • Assist in preparation, review, finalization, and distribution of study documents
    • Participate in study team meetings, take minutes, and track follow-up actions, decisions, risks to resolution
    • Support coordination of investigator payments and third-party vendor payments as needed
    • Contribute to contract and budget tracking under supervision of CPM
    • Create and maintain trackers, tools, and reports to monitor study metrics and document flow
    • Assist in training record tracking for study teams and site personnel
    • Engage with internal and external stakeholders (e.g., CROs, vendors, sites) professionally and proactively
    • Participate in department-wide process improvement or documentation initiatives

    Qualifications

    • BSc/BA degree in health care, life sciences or related field
    • Minimum of 4 years’ experience as a CTA in a pharmaceutical, CRO, or biotech environment in the context of pharmaceutical clinical trials
    • Familiarity with ICH-GCP, clinical trial life cycle, and document control and retention practices
    • Prior experience working in an outsourced study model or supporting vendor oversight preferred
    • Experience using electronic TMF systems and understanding of TMF Reference Model
    • Fluency in spoken and written English
    • Stakeholder management and communication skills

    Personal Qualities

    • Excellent verbal and written communication skills
    • Attention to detail and ability to manage multiple priorities independently
    • Proficiency in Microsoft Office (Word, Excel, Outlook, PowerPoint)
    • Solution-oriented mindset and proactive working style
    • Strong documentation and record-keeping abilities
    • Willingness to travel as required for business needs
    Mostra di più

    Position Snapshot


    Location: Vers-chez-les-Blanc, Switzerland

    Entity: Clinical Research Unit, Nestlé Research

    Work rate: 100%

    Contract type: Temporary

    Duration: 12 months


    Summary

    The Senior Clinical Trial Assistant (Sr. CTA) provides high-quality operational and administrative support to clinical trial teams throughout all phases of a pharmaceutical study. Operating within a fast-paced, regulated environment, the Sr. CTA ensures clinical documentation is accurately maintained, processes are followed, and systems are updated in a timely and compliant manner. This position works cross-functionally with internal stakeholders and external partners (e.g., CROs, vendors, investigator sites) to enable successful study execution in line with relevant pharmaceutical standards.


    ...

    Responsibilities

    • Support the Clinical Project Manager(s) in study execution, including tracking study milestones and key deliverables
    • Maintain and manage the Trial Master File (TMF/eTMF), performing periodic completeness and quality reviews
    • Assist in preparation, review, finalization, and distribution of study documents
    • Participate in study team meetings, take minutes, and track follow-up actions, decisions, risks to resolution
    • Support coordination of investigator payments and third-party vendor payments as needed
    • Contribute to contract and budget tracking under supervision of CPM
    • Create and maintain trackers, tools, and reports to monitor study metrics and document flow
    • Assist in training record tracking for study teams and site personnel
    • Engage with internal and external stakeholders (e.g., CROs, vendors, sites) professionally and proactively
    • Participate in department-wide process improvement or documentation initiatives

    Qualifications

    • BSc/BA degree in health care, life sciences or related field
    • Minimum of 4 years’ experience as a CTA in a pharmaceutical, CRO, or biotech environment in the context of pharmaceutical clinical trials
    • Familiarity with ICH-GCP, clinical trial life cycle, and document control and retention practices
    • Prior experience working in an outsourced study model or supporting vendor oversight preferred
    • Experience using electronic TMF systems and understanding of TMF Reference Model
    • Fluency in spoken and written English
    • Stakeholder management and communication skills

    Personal Qualities

    • Excellent verbal and written communication skills
    • Attention to detail and ability to manage multiple priorities independently
    • Proficiency in Microsoft Office (Word, Excel, Outlook, PowerPoint)
    • Solution-oriented mindset and proactive working style
    • Strong documentation and record-keeping abilities
    • Willingness to travel as required for business needs
    Mostra di più
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        published on 30 aprile 2026
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        <p>Du bist ein Organisationstalent, arbeitest gerne in einem sauberen Umfeld und möchtest einen Blick hinter die Kulissen der Lebensmittelentwicklung werfen? Für unseren Partner suchen wir für 6 Monate eine temporäre Verstärkung als</p>Hygieneassistent/in (w/m/d) 50%<p> </p><p>Werde Teil eines Teams, das täglich dafür sorgt, dass Qualität kein Zufall ist!</p><p>Deine Aufgaben im Labor und in der Produktion:</p><ul><li>Durchführung des Umwelthygienemonitorings in der Pilothalle</li><li>Probenahmen mittels Swabbing Technik von Oberflächen</li><li>Probenahme von Staub- und Pulverrückständen</li><li>Protokollierung der Proben und Eingabe ins Quality Management System</li><li>Verteilen und Versenden der Proben für die mikrobiologischen Analysen</li><li>Mithilfe bei der Probenvorbereitung und Auswertung der Analysenresultate</li></ul><p> </p><p> </p>
        published on 30 aprile 2026
      • Lab Technician Scientist in a QC Bioanalytical Lab

        • Schachen, Lucerna
        • Temporaneo
        <p>For one of our clients, a global pharmaceutical company in Schachen, we are looking for a Lab Technician Scientist in a QC Bioanalytical Lab to join their Biologics Analytical Department. <br /><br />The integrated Biologics Analytical Department provides support to the Biotechnology Department by performing release and stability testing of biological drug substances and is supporting global outsourcing of analytics for biologics, followed by study and quality monitoring to guarantee adherence to regulatory requirements and internal guidelines. Furthermore, the department conducts raw-/starting material and in-process testing for biological drug substances.<br /><br /> </p><p>General Information:<br /> </p><ul><li>Start date: ASAP</li><li>End date: 1 year </li><li>Extension: possible, to be discussed</li><li>Contract: temporary contract via Randstad</li><li>Workplace: Schachen, canton Lucerne</li><li>Workload: 100%</li><li>Working Hours: Standard</li><li>Home Office: Not possible, 100% on-site</li></ul><p> </p><p>Tasks & Responsibilities:<br /> </p><ul><li>Execution of analytical testing of drug substance release, stability and characterization for biologics under GMP/GDP</li><li>Support of analytical method validation and transfers, write technical protocols and report.</li><li>Troubleshoot methods to ensure seamless method qualification & execution in the laboratory</li><li>Support equipment maintenance, calibration and qualification & periodic review.</li><li>Works in accordance with applicable internal company regulations: safety, health and environmental protection.</li><li>Improvement of methods and troubleshooting around equipment and procedures.</li><li>Release and stability testing of biologics to determine relative potency according to cGMPs</li><li>Documentation of activities in an electronic laboratory notebook according to cGMPs</li><li>Supporting equipment maintenance and calibration activities</li></ul><p><br /><br />Requirements:<br /> </p><ul><li>Education as a laboratory technician EFZ or a scientific bachelor’s degree.</li><li>Work experience in a GMP laboratory.</li><li>Experience with biochemical analytical techniques and antibody biochemistry, binding assays, functional cell-based assays, PCR and/or with analytical testing with UPLC/HPLC, Capillary Electrophoresis, or other large molecule characterization techniques.</li><li>Experience with PAT (Process Analytical Technologies), spectroscopy and/or biopharmaceutical manufacturing processes is a plus.</li><li>Ability to communicate and document in English, communication skills in German is a plus.</li><li>Strong team player, demonstrating mutual respect.</li></ul><p><br />Sounds interesting? Apply now – we’re looking forward to receiving your applications!</p>
        published on 29 aprile 2026
      esplora le categorie correlate.
      • ricerca-e-sviluppo
      • chimici-microbiologi-e-tecnici-di-processo
      • tecnico-di-laboratorio

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