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Responsibilities:
- Responsible for compliance with regulatory and ICH guidelines.
- Independently serves as the lead point of contact for all data management study-related communications.
- Responsible for archiving trial(s) and associated documentation upon trial(s) completion.
About You:
- Bachelor's degree or equivalent in life science, computer science, or related discipline.
- Demonstrated proficiency in data management processes, clinical trial processes, and applicable regulatory requirements.
- Excellent organizational skills and attention to detail.
Adverum Biotechnologies, Inc.
Adverum Biotechnologies, Inc., a wholly owned subsidiary of Eli Lilly and Company, develops gene therapy as a new standard of care for ocular diseases. They are a clinical-stage company aiming to deliver therapies in physicians’ offices to eliminate the need for frequent ocular injections.