Associate Director, Medical Intelligence

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Company: Dermira, Inc.
Location: Menlo Park, CA 94025

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Associate Director, Medical Intelligence
Summary
Dermira (Nasdaq: DERM) is a publicly traded, commercial-stage company committed to developing new therapies for dermatologic conditions. Our marketed product, QBREXZA, is intended to reach the approximately 10 million people in the U.S. living with axillary hyperhidrosis, and we are initiating a Phase 3 trial for our biologic development candidate, lebrikizumab, for the treatment of moderate-to-severe atopic dermatitis.
We are looking for a talented, experienced and well-rounded Medical Affairs professional to provide Medical Intelligence Capabilities, reporting the Executive Director, Medical Information & Training.
What You Will Be Responsible For:
  • Establish literature surveillance capabilities and build/maintain a Dermira knowledge repository, including publication library, and ensure contribution and utilization by cross-functional colleagues
  • Perform critical analysis of internal/external literature and pro-actively develop/disseminate relevant Dermira and competitive product information to internal colleagues (electronically or via presentations)
  • Keep abreast of current scientific information regarding company’s marketed and investigational products and related competitors and act as a resource for the company working cross-functionally
  • Establish collaborative and positive working relationships with key internal stakeholders to inform literature surveillance capabilities and dissemination of analyses
  • Incorporate post-scientific congress information into Medical Affairs resources and disseminate to internal colleagues
  • Develop and maintain metrics on Medical Intelligence capabilities
  • Other responsibilities within Medical Affairs may be assigned
What We Need In the Role:
  • Advanced scientific degree (PhD, PharmD, MD)
  • 8+ years of related work experience in biopharmaceutical industry
  • Experience and knowledge in dermatology preferred
  • Ability to work independently with minimal supervision and collaboratively as a key contributor to multi-departmental teams
  • Demonstrated ability to manage many complex projects simultaneously
  • Prior leadership experience in Medical Affairs and reference database management
  • Ability to work in fast-paced environment in a hands-on manner while working collaboratively on multiple projects across product lifecycles
  • Strong technical writing and interpersonal skills; ability to interface and communicate effectively with other functions within the organization
  • Excellent judgment, critical-thinking skills and the ability to see problems and develop solutions to support business decision-making