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ICON plc

ICON plc iş ilanları Türkiye

Türkiye ICON plc 15 iş ilanı

  • ICON plc Turkey, Ankara

    Clinical Research Associate I/II at ICON plc: designing clinical trials, analyzing medical data & contributing to innovative treatments. · Conduct site qualification visits. · Evaluate protocol compliance & patient safety. · Collaborate with investigators & site staff. · ...

  • ICON plc Ankara

    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. · ...

  • ICON plc Istanbul, Istanbul

    We are currently seeking a · Clinical Research Associate I/II · to join our diverse and dynamic team. · What You Will Be DoingConducting site qualification, initiation, monitoring, and close-out visits for clinical trials. · ...

  • ICON plc Ankara

    We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, · interpreting complex medical data, and contributing to the advan ...

  • Contract Analyst

    1 hafta önce

    ICON plc Ankara

    We are currently seeking a Contract Analyst I to join our diverse and dynamic team. As a Contract Analyst I at ICON, you will prepare, negotiate and finalize agreements and budgets related to clinical trials and/or overseeing contract negotiations. · ...

  • Contract Analyst

    1 hafta önce

    ICON plc Turkey, Ankara

    We are seeking a Contract Analyst I to join our diverse and dynamic team. As a Contract Analyst I at ICON, you will prepare, negotiate and finalize agreements and budgets related to clinical trials. · ...

  • ICON plc Istanbul

    Clinical Research Associate I/II to join our diverse and dynamic team. Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. · Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. · Collaborating ...

  • ICON plc Ankara

    Clinical Site Associate (In-House CRA) at ICON plc: managing site-level communications, coordinating trainings and systems access, and supporting site readiness activities. · ...

  • ICON plc Ankara

    Clinical Research Associate II at ICON plc is responsible for designing and analyzing clinical trials, interpreting complex medical data and contributing to the advancement of innovative treatments and therapies. · ...

  • ICON plc Ankara

    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 ...

  • ICON plc Ankara

    +Negotiate and finalize Clinical Trial Agreements and amendments with sites across Turkey. · +Act as the primary contracting contact for Turkish sites, · +Maintain proactive communication with internal teams, · Job summary: Site Contracts Negotiator II will negotiate and finalize ...

  • ICON plc Ankara, Ankara

    Manage site-level communications and coordinate trainings for ICON plc's clinical research organization.Support monitoring tools to streamline trial operations and ensure data integrity. · ...

  • Senior CRA

    3 hafta önce

    ICON plc Turkey, Ankara

    We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. · Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. · Conducting site visits to ass ...

  • ICON plc Ankara

    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. · Manage site-level communications, · coordinate site trainings and systems access, · ...

  • ICON plc Ankara

    Manage site-level communications, coordinate site trainings and systems access, and support site readiness activities including pre/post site visit tasks. · ,Maintain Trial Master File (TMF) and Investigator Site File (ISF) accuracy and inspection readiness; · Support subject tra ...