Clinical Trial Operations Specialist

Perspective Therapeutics

United States

Remote

USD 50.000 - 75.000

Vollzeit

Vor 2 Tagen
Sei unter den ersten Bewerbenden

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Zusammenfassung

Perspective Therapeutics in the United States seeks a Clinical Trial Associate to provide comprehensive administrative support to the Clinical Operations Team. You will manage study documentation, support site outreach, coordinate meetings, and oversee the eTMF system to keep trials on track.

The role emphasizes compliance with ICH-GCP, meticulous record-keeping, and collaboration with cross-functional teams.

Qualifikationen

  • Bachelor's degree in life sciences or healthcare required.
  • Experience supporting clinical trials or healthcare operations preferred.
  • Familiarity with ICH-GCP guidelines.
  • Strong organizational and communication skills.

Aufgaben

  • Provide general administrative support to Clinical Operations and Project Management.
  • Assist ongoing conduct of studies and completion of required tasks to meet goals.
  • Attend meetings to assist with coordination and minutes generation.
  • Facilitate outreach to potential clinical trial sites and feasibility procedures.
  • Lead documentation checks and maintain eTMF progress.
  • Support creation of professional slide presentations for stakeholders.
  • Coordinate study material ordering, distribution, and tracking.
  • Organize data collection forms and ensure quality control as appropriate.
  • Assist in tracking and distributing correspondence and reports.
  • Coordinate document translation.

Kenntnisse

MS Word
MS Excel
PowerPoint
Outlook
GCP knowledge
Organizational skills
Team collaboration
English communication

Ausbildung

Bachelor's degree in life sciences or healthcare

Tools

eTMF system
Document management software

Jobbeschreibung

Perspective Therapeutics in the United States seeks a Clinical Trial Associate to provide comprehensive administrative support to the Clinical Operations Team. You will manage study documentation, support site outreach, coordinate meetings, and oversee the eTMF system to keep trials on track.

The role emphasizes compliance with ICH-GCP, meticulous record-keeping, and collaboration with cross-functional teams.

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