Eileen Brennan
Associate Director, Regulatory Affairs
- Role
- Associate Director Regulatory Affairs at ModeX Therapeutics Inc
- Location
- Boston, MA, US
- LinkedIn followers
- 500 followers
About Eileen Brennan
Biomedical professional with over fifteen years of clinical laboratory experience and a strong background in Quality Assurance, Regulatory Affairs, equipment management/operations, and maintaining compliance within GLP/GMP/GCP/GCLP/CLIA regulatory environments.
Experience
Associate Director Regulatory Affairs
Mar 2026 — Present
Education
Northeastern University
Master of Science - MS, Regulatory Affairs for Drugs, Biologics, and Medical Devices
2017 — 2020
University of Massachusetts Amherst
Bachelor of Science (BS), Microbiology, General
2000 — 2004
Skills
- Clinical Trials
- Elisa
- Hipaa
- Uv/Vis Spectroscopy
- Glp
- Laboratory Quality Assurance
- Microsoft Office
- Cell Culture
- Clinical Research
- Gel Electrophoresis
- Molecular Biology
- Fluorescence Microscopy
- U.s. Title 21 Cfr Part 11 Regulation
- Laboratory
- Gcp
- Biotechnology
- Protein Purification
- Western Blotting
- Pcr
- High-Performance Liquid Chromatography (Hplc)
- Capillary Electrophoresis
- CRO
- Tissue Culture
- Validation
- Life Sciences
- Microsoft Powerpoint
- Assay Development
- Computer System Validation
- Good Laboratory Practice (Glp)
- Flow Cytometry
- Research
- Software Development Life Cycle (Sdlc)
- Confocal Microscopy
- Edocs
- Polymerase Chain Reaction (Pcr)
- Standard Operating Procedure (Sop)
- Ich
- Transfection
- Veeva Vault
- Microsoft Excel
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