Responsibilities include screening/selection of molecules across various therapeutic segments & building a robust Product Pipeline, based on IP Challenges, product complexities and identifying opportunities and Innovative/ Niche dosage forms.
IQVIA Updation: GAP Analysis to be carried out to generate tailor made reports e.g. Dosage Form, Platform Technology, Therapeutic Category etc.
Tracking of the developments around Upcoming Technology, evolving Trends, & Mergers & Acquisitions.
Keeping a track of FDA Guidance's for Product Development, Peer ANDA approvals, Legal Updates & Drug Shortages. * 505b2 concepts: Identifying and creating differentiated 505b2 Pipeline Management of Clinical Trial & Pipeline Advocacy Screening various data sources such as Press Release, SEC Filings, Corporate Presentations & Clinical Trial Databases. Collating Data around different stages of development & maintaining CT Tracker. Portfolio Management
Build a Diversified Generic Portfolio with strategic focus on Exclusive First to File Opportunities, FTM/CGT/Priority Review & Limited Competition.
Providing Internal Governance to various Technical teams for Product Development, Pipeline Prioritization & Product Launch.
Work Experience 4-7yrs Education Masters in Pharmacy or Business Administration Competencies Collaboration Stakeholder Management Strategic Agility Developing Talent Result Orientation Innovation & Creativity Customer Centricity Process Excellence