Sheryl Littmann
Drug Development | Medical Writing | Project Management
- Role
- Associate Director, Medical Writing at Spyre Therapeutics
- Location
- New Rochelle, NY, US
- LinkedIn followers
- 500 followers
About Sheryl Littmann
Experienced drug development and project manager in the life science industry. Accomplishments in the project management, regulatory, pharmacovigilance, clinical research and quality assurance and auditing areas. Develop process improvements most notably in labeling, regulatory submissions, pharmacovigilance, medical writing and quality. Lean six sigma green belt certified.Specialties: Project Management | Regulatory Submissions | Labeling | Regulatory and Medical Writing| Pharmacovigilance | Clinical Research and Development| Quality Assurance and Auditing |Team Training | Continuous Improvements| Cross Functional Team Management
Experience
Associate Director, Medical Writing
Jan 2025 — Present
Education
Rutgers University
BS, Biology
Fordham University
MBA, Global Professional MBA in Marketing and Finance
Skills
- Medical Writing
- Cross-Functional Team Management
- Clinical Development
- Sop Development
- Process Development & Improvement
- Pharmaceutics
- Biotechnology
- Clinical Trials
- Pharmaceutical Industry
- Sop
- Fda
- Strategy
- Quality Assurance
- Pharmacovigilance
- Regulatory Submissions
- Standard Operating Procedure (Sop)
- Regulatory Requirements
- Drug Development
- Project Management
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