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Site Management:
- Assist with investigator recruitment, site selection, startup, and close-out tasks.
- Provide ongoing operational support to sites via phone and email.
Regulatory and Data:
- Track essential regulatory documents and ISF for audit readiness.
- Maintain eTMF and resolve EDC data queries.
Monitoring and Compliance:
- Conduct qualification, initiation, interim, and close-out visits in person or remotely.
- Verify source data, ensure GCP/FDA compliance, and escalate protocol deviations.
Qualifications:
- Requires a life science degree and 2+ years of clinical research experience.
- Willingness to travel up to 30%.
Lycia Therapeutics
Lycia Therapeutics is a clinical-stage biotechnology company developing LYTAC-based therapeutics to degrade disease-driving proteins. It went public in 2026 and is headquartered in South San Francisco, California.