Cta

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Experience with clinical documentation
Knowledge of good clinical practice
Proficient in microsoft office suite
Assist Clinical Research Associates and Regulatory teams with clinical documents

Job Summary

  • Assist Clinical Research Associates and Regulatory teams with clinical documents.
  • Act as a central contact for project communications and documentation.
  • May accompany CRAs on site visits to assist with monitoring duties.

Matching Summary

Assist Clinical Research Associates and Regulatory teams with clinical documents.

Skills & Requirements

Must-have

  • Experience with clinical documentation
  • Knowledge of Good Clinical Practice
  • Proficient in Microsoft Office Suite

Nice-to-have

  • Strong organizational skills
  • Effective communication abilities
  • Ability to work in a team environment

Key Requirements

  • Bachelor degree and above
  • 1-3 years administrative support experience
  • Awareness of clinical research regulatory requirements

Work Rights

Not specified

Tailored Resume

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