Job Description

Duration: 6 months

Commitment: 40 hours per week

Location: Onsite 5 days a week in Palo Alto

Responsibilities:

• Manage and process clinical safety events, including timely assessment, coding (MedDRA), and reporting
• Collaborate across clinical teams to ensure accurate and complete safety data
• Draft safety narratives and prepare materials for safety review boards (e.g., DSMB, CEC)
• Contribute to safety sections of interim, annual, and final clinical reports
• Support cross-functional efforts with external partners and internal departments
• Participate in safety vigilance activities aligned with regulatory requirements
• Provide administrative and training support during clinical study start-up
• Ensure data accuracy and protocol adherence through continuous quality oversight
• Exhibit critical thinking, proactive problem-solving, and effective cross-team collaboration

Requirements:

• 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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