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Medical Affairs Director

1 month ago

Foster City, California, United States LanceSoft, Inc. Full time
Job Title: Medical Affairs Manager

Join LanceSoft, Inc. as a Medical Affairs Manager and contribute to the development and execution of global strategies for products in the LIFE franchise.

Key Responsibilities:
  • Collaborate with internal and external stakeholders to develop and execute global strategic activities.
  • Develop and present presentation materials for internal and external meetings, including Advisory Boards.
  • Provide medical and scientific expertise to colleagues, including medical educational activities, grants, and investigator-sponsored/collaborative studies.
  • Support data generation activities through critical review of global ISRs, Ph 3b, and Ph4 study proposals.
  • Manage HBV Phase IV portfolio, including liaising with key cross-functional partners.
  • Review abstracts and/or manuscripts resulting from the phase IV program.
  • Support the management and documentation of phase IV study status.
  • Serve as Medical Affairs therapeutic area expert on Global Publications and Scientific Message Platform committees.
  • Provide medical and scientific coverage and support at key scientific meetings.
  • Support project leads in the execution and tracking of their projects.
  • Oversee medical and scientific review of promotional materials for GRC and MRC.
Requirements:
  • Demonstrate deep subject matter expertise with regard to LIFE products and competitive products.
  • Excellent written, verbal, and interpersonal communication skills.
  • Excellent organizational skills to support project planning across multiple activities.
  • Excellent teamwork skills, with the ability to meet timelines in a fast-paced environment.
  • Excellent analytical and problem-solving skills, with the ability to identify and understand complex issues and problems.
  • Experience in public health or Internal Medicine (general or subspecialty) is highly desirable.
  • Experience in developing effective abstracts, manuscripts, posters, and slides, and presenting at scientific meetings.
  • Must be fully cognizant and adhere to regulatory and legal requirements for clinical trials and other Medical Affairs activities.
  • Must be able to work with autonomy and independence.
  • Ability to work around international time zones and ability to travel to and participate in domestic and international conferences.
Qualifications:
  • Bachelor's degree a minimum, but M.D., D.O., PhD (biological or pharmaceutical sciences), or PharmD preferred.
  • Preferred experience in Medical Affairs and/or Clinical Research, including Phase IIIb and IV studies.