Clinical Trial Safety Scientist (permanent Home Based)

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Base: zł102,800.00 - zł272,500.00; bonus/equity: n...
Review clinical/safety data
Medical accuracy and completeness
Generate applicable queries
Ensure consistent processes and efficient review of critical clinical/safety data on an ongoing basis

Job Summary

  • Ensure consistent processes and efficient review of critical clinical/safety data on an ongoing basis.
  • Contribute to study start-up activities and serve as a member of the Extended Study Team.
  • Provide input into the process of setting automated and handwritten patient narratives.

Matching Summary

Ensure consistent processes and efficient review of critical clinical/safety data on an ongoing basis.

Salary

Base: zł102,800.00 - zł272,500.00; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • Review clinical/safety data
  • Medical accuracy and completeness
  • Generate applicable queries
  • Contribute to study start-up
  • Report on TRISARC deliverables
  • Escalate urgent medical cases
  • Lead quality of own deliverables

Nice-to-have

  • Quality focus and analytical skills
  • Concise summarization of complex info
  • Work cross-functionally
  • Global studies experience

Key Requirements

  • Minimum 4+ years of experience in Pharmacovigilance / Drug Safety
  • Educational degree (BSc/Msc/PhD) in Life Science or equivalent
  • Understanding of clinical study and drug development process
  • Knowledge of ICH/GCP Guidelines
  • Knowledge of SAE reporting requirements
  • Experience using data review tools is preferred

Work Rights

Not specified

Tailored Resume

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