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Pharm D Elizabeth Johnson

Director, US Medical Information

Executive Summary & Candidate Overview

Pharm brings a wealth of experience in medical information management, pharmaceutical content development, and regulatory compliance. As a Director of US Medical Information, he has led teams in establishing processes, overseeing department needs, and ensuring compliance with regulatory standards. Pharm's proficiency in medical review, scientific writing, and software utilization has been instrumental in driving the success of pharmaceutical companies.

Accomplishments and Key Performance Indicators (KPIs)

Pharm has successfully led various initiatives in medical information management, including the establishment of standard response databases, rollout of medical information systems, and development of medical content deliverables. His contributions have led to improved efficiency, enhanced customer satisfaction, and compliance with regulatory requirements. Pharm's ability to manage teams, provide strategic guidance, and collaborate with key stakeholders has been key to his success in the pharmaceutical industry.

Location and Travel
  • Open to: On-site roles.

  • Remote Roles: Willing to consider opportunities based on specific position requirements.

  • Compensation Seeking: Open to discussing compensation details upon scheduling a meeting.

  • Position Seeking: Seeking leadership roles in medical information management, pharmaceutical content development, and regulatory compliance within the pharmaceutical industry.

Work Experience
  1. Director, US Medical Information - Valeant Pharmaceuticals (May 2017 – Present)

    • Established processes for medical inquiries fulfillment and oversaw department needs.

    • Led the rollout of medical information systems and collaborated with key stakeholders.

    • Actively participated in FDA audits and managed relationships with global medical counterparts.

  2. Associate Director, Medical Content - Bristol-Myers Squibb (April 2016 – May 2017)

    • Managed external agencies and internal stakeholders for content deliverables.

    • Provided guidance on medical content development and budget planning for launch preparation.

    • Collaborated with global medical teams on the development of medical content for tumor launch.

  3. Associate Director, Medical Information - Otsuka America Pharmaceutical Inc (February 2012 – April 2016)

    • Led the creation of standard response databases and ensured medical information needs were met.

    • Managed, coached, and provided strategic guidance to team members on medical responses.

    • Liaised with internal and external stakeholders on medical insights and formulary review decisions.

  4. Consultant/Manager/Senior Manager, Medical Information - Bristol-Myers Squibb (May 2006 – January 2012)

    • Developed and maintained letter databases for various pharmaceutical products.

    • Participated in medical review committees and provided medical information responses to customers.

    • Trained incoming contractors on medical information systems and processes.

  5. Analytical Chemist - Schering Plough (May 2000 – June 2001)

    • Conducted quality control tests and performed dissolution for pharmaceutical products.

    • Utilized laboratory equipment and adhered to USP standard procedures.

  • Doctor of Pharmacy in Pharmacy University of the Sciences in Philadelphia, Philadelphia, PA

  • Bachelor of Arts in Chemistry Rutgers University, Douglass College, New Brunswick, NJ

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Pharm D Elizabeth Johnson
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