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Clinical Safety Associate

Clinical Safety Associate

LumicityPalo Alto, CA, US
30+ days ago
Job type
  • Full-time
Job description

Company : Medical Device

Duration : 6 months

Commitment : 40 hours per week

Location : Onsite 5 days a week in Palo Alto

Key Responsibilities :

  • Manage and report clinical safety events (incl. MedDRA coding)
  • Ensure accurate safety data through cross-team collaboration
  • Draft safety narratives and review board materials
  • Contribute to safety sections of clinical reports
  • Support study start-up, training, and regulatory compliance
  • Maintain data quality and protocol adherence

Qualifications :

  • MD or MBBS Degree REQUIRED
  • Some clinical trial or research experience within a biotechnology, pharmaceutical, or medical device company
  • Strong experience with Microsoft Office

    • No C2C

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    Clinical Associate • Palo Alto, CA, US

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