Associate Director – Global Regulatory Policy & Strategy

Posted 46ds ago

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Job Description

Associate Director for Global Regulatory Policy & Strategy supporting multiple U.S. regulatory policy campaigns and building Lilly policy positions to effectuate change. Collaborating with stakeholders to improve patient outcomes in drug development.

Responsibilities:

  • Support Multiple Regulatory Policy Campaigns
  • Lead the development of Lilly policy positions in coordination with internal subject matter experts (i.e., problem statements and desired future state)
  • Collect data and/or conduct research to support company policy positions
  • Perform stakeholder analyses to understand external perspectives on key Lilly policy priorities
  • Track, monitor, and provide analysis of relevant regulatory policies, as advised by management
  • Monitor the external environment for new regulatory and policy developments and possible implications for Lilly’s positions and connect with internal stakeholders
  • Develop and Execute Policy Strategy and Plans
  • Support the development and implementation of tactical policy plans, including a description of both short- and long-term project deliverables
  • Contribute to the development and execution of global regulatory policy strategies that align with Lilly’s long-term business objectives and external policy landscape
  • Exert External Influence
  • Develop relationships with key external stakeholders to understand their perspectives and advise them regarding Lilly’s positions
  • Represent Lilly in external forums, including regulatory agency meetings, trade associations, and policy roundtables.
  • Impact patient outcomes through collaboration across partner groups
  • Effectively Lead, Engage, and Partner
  • Exemplify Team Lilly behaviors in internal and external interactions
  • Model innovation and leadership behaviors and regulatory excellence attributes as described in Global Regulatory Affairs white papers
  • Engage in forums that share regulatory information across GRA components and other Lilly teams and business partners

Requirements:

  • Bachelor's Degree in policy, public health, regulatory, clinical, legal, business, research, science or related field
  • 2+ years prior regulatory/policy experience
  • Qualified applicants must be authorized to work in the United States on a full-time basis
  • Masters, doctorate or advanced degree is preferred
  • 3+ years of regulatory/policy experience is preferred
  • Travel up to 25%
  • Strong interpersonal skills and demonstrated ability to manage external and internal relationships with key stakeholders
  • Ability to research and write briefings, positions, and high-level communication
  • Independence, resourcefulness, influence without authority
  • Strong communication skills, both verbal and written.

Benefits:

  • eligibility to participate in a company-sponsored 401(k)
  • pension
  • vacation benefits
  • eligibility for medical, dental, vision and prescription drug benefits
  • flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts)
  • life insurance and death benefits
  • certain time off and leave of absence benefits
  • well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities)