PSI CRO AG
PSI CRO AG
PSI CRO AG este o organizație globală de cercetare contractuală care sprijină studiile clinice, cu accent pe studiile esențiale de fază 2 și fază 3. Activitatea sa acoperă domenii terapeutice precum bolile inflamatorii intestinale, oncologia, hematologia, bolile infecțioase, scleroza multiplă și bolile rare. Compania utilizează o platformă proprie pentru planificarea studiilor clinice și monitorizarea financiară, ajutând echipele să urmărească termenele și bugetele studiilor. Profilul PSI CRO AG combină expertiza în domeniul sănătății și consultanței, punând accent pe calitate, compatibilitate și desfășurarea fiabilă a studiilor.

Clinical Research Associate I, UK Remote

Support clinical trials across the United Kingdom through onsite monitoring, site management, data review, and regulatory coordination. This role focuses on participant safety, data quality, investigator relationships, and effective communication with study stakeholders.

Descriere

  • Conduct and document all types of onsite monitoring visits
  • Contribute to study startup activities when required
  • Review case report forms, verify source documents, and resolve data queries
  • Coordinate communication with clinical sites
  • Act as a contact for internal support functions and external vendors
  • Update internal project teams on study progress
  • Contribute to feasibility assessments
  • Assist regulatory colleagues with study submission documentation
  • Develop and maintain relationships with clinical sites and investigators
  • Safeguard participant rights, safety, and well-being while supporting data quality compliance

Cerințe

  • University or college degree in life sciences, or an equivalent combination of education, training, and experience
  • Experience in clinical research or medicine
  • Independent onsite monitoring experience in the United Kingdom
  • Proficiency with Microsoft Word, Excel, and PowerPoint
  • Ability to plan effectively, manage multiple priorities, and contribute in a fast-paced team environment
  • Strong communication, collaboration, and problem-solving abilities
  • Willingness and ability to travel
  • Valid driver's license

Beneficii

  • Remote work arrangement
  • Full-time position
  • Guidance from an experienced and professional team
  • Opportunities to broaden professional skills
  • Career development opportunities within the company
  • Participation in challenging, full-scale clinical research projects

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