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Associate Director – Lead
Protocol Review Committee, Prc
Posted on 8/3/2022
INACTIVE
Locations
Toms River, NJ, USA • Princeton, NJ, USA
Experience Level
Entry
Junior
Mid
Senior
Expert
Desired Skills
Leadership
Management
Responsibilities
  • Process owner for 1-2 TA specific PRC(s)
  • Facilitate each Asset Teams journey through PRC review to ensure team readiness, appropriate review, clear documentation of decisions/approvals and process efficiency
  • Manage projects related to the ongoing implementation and continuous improvement of the PRC process
  • In coordination with the CoE Head and partnering with BI&A, develop, refine and report outcome-based metrics for the PRCs
  • Manage other initiatives related to Quality and the Governance process
  • Help develop norms and standards, including best practices in meeting management and guidance for participants in processes, to be shared across GDD
  • Partner with QMS and governance to align with overall quality process strategy and execution
  • Use appropriate change management and communication principles
Desired Qualifications
  • Advanced degree (MA, MS, MBA, PhD, etc.) and 5+ years of biopharma industry experience
  • Strong project management experience in the biopharma industry; PMP certification is desirable
  • Strong oral and written communications skills, as well as strong analytical ability
  • Demonstrated ability to build relationships, influence, negotiate and drive organizational engagement
  • Ability to handle multiple concurrent projects in a dynamic and challenging environment
  • Flexibility to adapt to changing needs of the organization
  • Understanding of relevant opportunities, interdependencies and complex trade-offs
  • Ability to manage multiple stakeholders, competing priorities and navigate uncertainty across the matrix
  • Experience in process management, continuous improvement and leading matrix leadership teams a plus
Bristol-Myers Squibb

10,001+ employees

Biopharmaceutical development company
Company Overview
Bristol-Myers Squibb engages in the discovery, development, licensing, manufacturing, marketing, distribution and sale of pharmaceuticals.