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    Clinical Trial Coordinator - São Paulo, Brasil - Fortrea

    Fortrea
    Default job background
    Tempo integral
    Descrição
    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 conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.

    Main responsibilities:

    Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investigator and essential documents for a study and any other local applications are made within the timelines agreed with project management and Site Readiness team and that documentation meets the specifications required by applicable regulations and sponsor.

  • Preparation and follow-up of formal and informal imports processes
  • Vendors contracts
  • Vendors payment processes, forecast and invoices review/approval
  • Coordination of POs and vendor ́s control spreadsheets
  • Post in Veeva Vault/eTMF the Import, export, and local purchase documents
  • Update and Management of SAP
  • Post Study supply Coordination, medication purchase and shipment to the sites
  • Complaint tracker filling (import and local purchase) for temperature deviations
  • Contact local purchase vendor in cases of temperature deviations at site
  • Participating in project meetings
  • Requirements:

    Previous experience in clinical development working with Impots & Supply-chain or Procurement
    Demonstrated understanding of research protocol requirements and proven ability to communicate with/educate others about them.

    University/College degree (life science preferred), or certification in a related allied health profession from an appropriate accredited institution (e.g., nursing certification, medical or laboratory technology)

    Fluent English

    Labcorp is proud to be an Equal Opportunity Employer:

    As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.

    For more information about how we collect and store your personal data, please see our .



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