Proj Mgr, Clinical Supplies

hace 4 semanas

Santiago de Chile Thermo Fisher Scientific A tiempo completo

Supports supply chain for moderate complex global clinical trials. Ensures project/study activities are in compliance with company and client requirements. May act as a representative and project lead for the department on less complex projects.
- Develops study specific plans for each assigned project.
- Meets with internal teams to coordinate efforts, provide recommendations and risks, and update project reports/spreadsheets.
- Ensures fluent communication and interaction between internal departments in order to avoid obstacles during the course of the study.
- Integrates all clinical supplies activities into the supply chain to support project logistic strategy and compliance with GxP requirements.
- Participates in ongoing training on new regulations.

  • Senior Specialist

    hace 3 semanas

    Santiago, Chile Fortrea A tiempo completo

    The Clinical & Ancillary Supplies Services (CASS) Senior Specialist: Coordinate and oversee aspects of logistics related to Clinical and Ancillary Supplies services. Support these services to both internal and external clients. Responsible for the set-up and coordination of project activities related to clinical and ancillary supplies Independently...

  • Cta

    hace 6 días

    Santiago de Chile IQVIA A tiempo completo

    Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...

  • Sr Cra

    hace 4 semanas

    Santiago de Chile Fortrea A tiempo completo

    As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

  • Cra I

    hace 3 semanas

    Santiago de Chile Labcorp A tiempo completo

    Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Essential Job Duties: 1) Responsible for all aspects of study site monitoring including routine monitoring and closeout of clinical...