Carrie Mazzrillo
- Role
- Director at Vertex Pharmaceuticals
- Location
- Framingham, MA, US
- LinkedIn followers
- 500 followers
About Carrie Mazzrillo
Extensive strategic project management of Global Dossiers including development and…
Experience
Director
Aug 2021 — Present
Manages team with various levels of experience to ensure both company goals and individual growth opportunities are met • Partner with Therapeutic Regulatory Lead and submission team to develop regional and global submission strategies to support decision-making in order to ensure high quality and on-time submissions. • Maintain critical project/submission timelines by developing timelines, tracking deliverables, milestones and metrics and identifying and resolving issues. • Provide guidance and technical feedback for project related issues for global and regional major applications and CMC, Clinical and Nonclinical lifecycle submissions. • Facilitate the definition of the project milestones, tasks, deliverables, key dependencies and resource requirements. • Develop and maintain project plans, status reports, issue logs, and other project related artifacts • Identify & facilitate strategies for risk mitigation and contingency planning. • Effectively communicates project status, issues, schedule and accomplishments to various management and stakeholder groups, as needed. • Prepares necessary reports to drive data driven resource, budget and trade-off discussions across GRA function. • Attend and participate in industry functions, panels, and development groups to increase knowledge of eCTD and other regulatory requirements.
Education
University of Phoenix
MBA, Business Administration
2005 — 2007
Excelsior University
BS, Psychology
2004 — 2005
Skills
- Situational Leadership
- Drug Development
- Documentum
- Emotional Intelligence
- Clinical Development
- Compliance
- Cross-Functional Team Leadership
- Ind
- Microsoft Office
- Sop
- Project Management
- Adobe Acrobat
- Quality Assurance
- Business Process
- Change Control
- Fda
- Validation
- Pharmaceutical Industry
- Global Dossier
- Document Management
- Process Improvement
- Ectd
- Regulatory Submissions
- Regulatory Affairs
- Pharmaceuticals
- Word
- Nda
- Edc
- Documentation
- CRO
- Situational Self Leadership
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