Kerri Stone
Business and Project Operations
- Role
- Sr Project Manager at ICON plc
- Location
- Reading, MA, US
- LinkedIn followers
- 500 followers
About Kerri Stone
A highly effective operations and project manager with over 20 years of experience in the pharmaceutical, medical device and biotechnology industries. Expertise in managing and coordinating multiple projects from initiation to closure, including proposal development, contracting, resource management, and project management.Excellent organizational and interpersonal skills for the management of large to small teams. Able to work independently or as part of a team. Knowledge of Good Clinical Practices (GCP), Good Manufacturing Practices (GMP), and Quality System Regulation (QSR) regulations and requirements.
Experience
Sr Project Manager
May 2020 — Present · Reading, MA, US
Oversees the project management program within Strategic Regulatory Services Department.Responsible for managing projects to successful outcomes by ensuring project objectives are achieved within time, cost and quality standards.Contributes toward culture of business excellence with a focus on streamlining processes, adding value to the business and exceeding client needs.Primary point of contact for designated projects, responsible for: delivering successful working relationships with clients, cross functional project planning, scheduling and implementation, defining project scope, resource requirements and deliverables, risk migration strategies, associated action plan and issue resolution.Manages projects in accordance with contract including: budget, invoicing procedures, monitoring and reporting on progress of projects to stakeholders and implementing QC activities as needed.
Education
UMass Boston
Bachelor's degree, Elementary Education, Psychology
1988 — 1992
Suffolk University
Masters, Public Administration/Concentration in Health Administration
1993 — 1996
Skills
- Medical Devices
- Capa
- Quality Assurance
- Standard Operating Procedure (Sop)
- Quality Control
- Gmp
- Quality System
- V&V
- 21 Cfr Part 11
- Gcp
- U.s. Title 21 Cfr Part 11 Regulation
- Six Sigma
- Change Control
- U.s. Food and Drug Administration (Fda)
- Validation
- Clinical Development
- Pharmaceutical Industry
- Sop
- Fda
- Biotechnology
- Technology Transfer
- Regulatory Affairs
- Clinical Trials
- Vaccines
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