Thermo Fisher Scientific
Thermo Fisher Scientific
Thermo Fisher Scientific dezvoltă și furnizează tehnologii, produse de laborator și servicii farmaceutice care sprijină cercetarea științifică și asistența medicală. Activitatea sa acoperă cercetarea în domeniul științelor vieții, rezolvarea problemelor analitice, creșterea productivității laboratoarelor, diagnosticarea, precum și dezvoltarea și producția de terapii. Compania își deservește clienții printr-o echipă globală și un portofoliu de mărci care include Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon și PPD. Oportunitățile de carieră includ activitățile științifice, medicale, de producție, logistice și de servicii care susțin aceste oferte.

Remote Clinical Trial Coordinator in Argentina

Support clinical trial site activation, regulatory documentation, feasibility work, and site communications for a global clinical research organization. Maintain trial systems, study files, metrics, and investigator site materials.

Descriere

  • Coordinate assigned clinical trial activities in line with the task matrix
  • Review departmental, internal, country, and investigator files and document findings
  • Deliver assigned work on schedule, within budget, and to required quality standards
  • Support Activate and eTMF systems while keeping study databases up to date
  • Process Client (e)TMF documents, complete reviews, distribute communications, and prepare reports
  • Analyze and reconcile study metrics and findings reports
  • Coordinate and distribute Investigator Site File materials, pharmacy binders, and study supplies
  • Support translation materials and perform translation quality checks
  • Stay current on SOPs, client instructions, and applicable regulatory guidance
  • Assist with client and internal meeting coordination, regulatory tracking, and RBM activities
  • Maintain study records, training logs, system access, team lists, and activity plans
  • Submit documents to clients and centralized IRB/IEC bodies
  • Maintain vendor trackers and assist with regulatory submissions
  • Work with sites to collect site-selection documentation
  • Assemble regulatory compliance review packages
  • Coordinate with internal teams to align site start-up activities
  • Complete Site Interest Plans and collect site documentation when required
  • Record site communications, follow-ups, and survey responses in real time
  • Check survey data for logical consistency, completeness, and accuracy
  • Work with teammates and clinical staff to address site issues and risks
  • Monitor site-contact plans and escalate concerns or non-compliance
  • Apply local knowledge of site capacity and experience to recommend additional sites
  • Partner with Global Investigator Services to resolve investigator questions and maintain contact details
  • Contribute to global feasibility workflows and continuous improvement practices
  • Train new team members on relevant processes and systems
  • Use local market knowledge to identify and develop new clinical trial sites

Cerințe

  • High school or secondary diploma, or equivalent, plus relevant academic or vocational training
  • Comparable professional experience of 0–1 year
  • Bachelor’s degree preferred
  • Strong English communication and grammar skills, with local-language proficiency where required
  • Proficiency with Microsoft Word, Excel, and PowerPoint
  • Capacity to learn and use clinical trial database systems
  • Working knowledge of applicable country regulations, ICH Good Clinical Practice, and organizational or client SOPs and WPDs
  • Ability to complete the organization’s clinical training program successfully
  • Accuracy in following project work instructions
  • Ability to identify risks and escalate them appropriately
  • Occasional driving to site locations and potential occasional travel required

Beneficii

  • Fully remote work arrangement
  • Full-time employment
  • Standard Monday–Friday schedule
  • Potential occasional travel
  • Training and onboarding support

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