Related skills
data management project management microsoft office study coordination glp📋 Description
- Support the Study Director in developing study protocols, amendments, and related documentation.
- Facilitate cross-functional communication; track study timelines and milestones.
- Identify and help eliminate roadblocks delaying study progress.
- Assist with implementation of test methods and SOPs described in the study protocol.
- Ensure experimental data are accurately recorded and verified.
- Manage the study schedule and alert the team to critical data collection points or deadlines.
🎯 Requirements
- Bachelor's degree in biology, neuroscience, biomedical engineering, animal science, or related field.
- At least 1 year of preclinical research support, study coordination, or project management.
- Solid understanding of GLP (21 CFR Part 58) and ISO 10993; in vivo studies experience.
- Strong organizational and project management skills; able to manage timelines and priorities.
- Attention to detail; proficient in data compilation, documentation, and MS Office.
- Experience in animal research facilities with IACUC protocols.
🎁 Benefits
- Growth potential with opportunities for impact.
- Comprehensive medical, dental, and vision insurance.
- Paid holidays and commuter benefits.
- Meals provided.
- Equity (RSUs) for full-time employees.
- 401(k) plan.
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