Clinical Safety Associate Job at Lumicity, Palo Alto, CA

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  • Lumicity
  • Palo Alto, CA

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**

Job Tags

Interim role,

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