Abstract
Ensuring that a product is brought to market quickly, safely, and cheaply is crucial for any pharmaceutical company. Driving a product to "first to market” is not an easy endeavor, and it is the aspiration of each pharma company.
Project managers work across the industry, from research and development to commercialization, to promote efficiency to achieve the business goals. From risk mitigation, to change management, to stakeholder manager, project managers fluidly embrace the fast-paced competitive landscape in pharma companies to support success of product launches ensuring patients receive the treatments they need.
This talk touches on the skills and application of PM methodology to understand how to drive the success and manage high value projects in pharmaceutical companies.
Learning objectives:
- Learn about how project management skills are utilized in the pharmaceutical industry – including in clinical operations, commercial operations and delivering high value for the success of the business.
- Learn key ways that PM applies Stakeholder Management, Risk Management, and additional strategic management within pharma
- Understand key future trends in PM
Registration
- $0.00 - PMINJ Chapter members
- $5.00 - Non-members (no refund)
- The link to the virtual meeting will be included in
the Registration Receipt
- Download the Zoom app at: https://zoom.us/download
Speaker
Hannah Javed, MBS is a Manager of Project Management at Teva Pharmaceuticals, a global leader in generics, biosimilars, and innovative medicines. She has a Master's degree in Biomedical Sciences from Rutgers University and a passion for providing the best therapeutics for patients everywhere.
In her current role, she supports the Teva NA Commercial division by managing projects to optimize organizational performance. She drives change management efforts, mitigates risks and roadblocks, and ensures alignment of stakeholders. She has experience in various systems and tools, such as Veeva Vault, COSMOS, Microsoft Excel and PowerPoint, and FDA Regulatory Documentation Management. She also has a background in clinical trial operations, documentation, and compliance, working with eTMF and various therapeutic areas.
Hannah is a strong professional with skills in interpersonal, operations, and strategic project management. She was also a mentor for the Early Talent Summer Internship Program at Novo Nordisk, where she previously worked as a Senior Clinical Trial Associate and a Senior Associate - Site Management Documentation. She values learning and growing from her mentors and peers and sharing her knowledge and experience with others.
