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**

Interim role,