Clinical Safety Associate

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**