Clinical Trial Safety Scientist (permanent Home Based)

Ivivamedical

Base: zł102,800.00 - zł272,500.00; bonus/equity: n...
Review clinical/safety data
Medical accuracy and completeness
Coding consistency
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.
  • Prepare aggregated data visualization and facilitate meetings related to review of safety data on study level.
  • Serve as a member of the Extended Study Team and report on TRISARC deliverables.

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
  • Coding consistency
  • Generate applicable queries
  • Study level safety data review
  • Contribute to study start-up
  • Report on TRISARC deliverables
  • Escalate urgent medical cases

Nice-to-have

  • Quality focus
  • Analytical skills
  • Concise summarization
  • Cross-functional work
  • Global studies
  • Different phases of development

Key Requirements

  • BSc/Msc/PhD in Life Science or equivalent
  • Minimum 4+ years of experience in Pharmacovigilance / Drug Safety
  • 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
  • Proven ability to prioritize and manage multiple tasks
  • Excellent time management
  • Very good interpersonal and communication skills
  • Team player, able to work individually

Work Rights

Not specified

Tailored Resume

Cover Letter