88-50101989 Therapeutic Area Pipeline Medical Science Liaison

Roche•South San Francisco, CA
•$242,712 - $299,500•Remote

About The Position

Genentech, Inc. seeks a Therapeutic Area Pipeline Medical Science Liaison at its South San Francisco, CA location. Within a global pharmaceutical company, serve as a field medical partner responsible for providing clinical, scientific, and other relevant information related to disease states and the appropriate utilization of Genentech medicines in Immunology/Inflammatory Bowel Disease (IBD). This includes information on the therapeutic area pipeline and TA-related approved medicines. The role is responsible for managing Phase I-III pediatrics and adult clinical trials in the assigned geographic area, supporting site identification, start-up, clinical trial recruitment, and study retention. The position ensures an end-to-end customer experience by building and leveraging relationships with investigators, site staff, and clinical operations partners to enable and expedite the successful delivery of clinical development programs within IBD. The liaison will engage with healthcare providers, clinical study staff, therapeutic area experts (TAEs), population health decision makers, and patient thought leaders within their region(s) to further patient outcomes aligned with Genentech's objectives. This role involves identifying educational gaps and providing real-time insights and ground-level understanding of the IBD Disease Area across US Regions and countries to inform strategies. The position partners with U.S. cross-functional colleagues and global teams, developing and managing projects that can improve the care of underserved populations. In collaboration with home office and regional partners, the role is accountable for comprehensive activities focused on delivering a successful clinical development program, including clinical trial recruitment activities, competitive intelligence, Congress support, professional society engagement, and TA landscaping. The role is responsible for covering multiple pipeline medicines, engaging in broad clinical and scientific discussions, and sharing customer insights with key stakeholders. Additionally, the position serves as a Point of Contact (PoC) for AI and Digital Strategies, leading internal initiatives and discussions regarding the efficient, ethical, and proper use of artificial intelligence solutions, improvements in digital tools supporting field activities, and leveraging field medical strategy.

Requirements

  • Bachelor’s degree, or foreign equivalent, in Pharmaceutical or Clinical Sciences or related field and 5 years of progressive, post-baccalaureate experience in job offered, or Medical Manager/Leader/Partner, or related position in the pharmaceutical industry.
  • Alternatively, a Master’s degree, or foreign equivalent, in fields specified and 3 years of the specified experience.
  • Two (2) years of experience must include: Pipeline development experience in Immunology; Inflammatory Bowel Disease, Ulcerative Colitis, and Crohn’s Disease
  • Experience with immunomediated diseases, neurology, rare diseases, renal, and onco-hematology therapeutic areas
  • Launch Readiness and Clinical-to-Commercial Transition
  • End-to-end lifecycle management of IBD pipeline molecules, including Phase I to IV trial support and HEOR integration
  • Solid understanding of the US Healthcare System, management, and care of IBD patients in the United States
  • Proficiency in GCP (Good Clinical Practice) and ICH (International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use)
  • Relevant therapeutic area knowledge, comprehensive understanding of product and safety profiles, and familiarity with managed care, health economics, reimbursement, and legal and regulatory landscape in the pharmaceutical/biotechnology industry.
  • In-depth knowledge of clinical development programs and clinical trial management
  • Experience with the management of Pediatric Trials

Responsibilities

  • Serve as a field medical partner providing clinical, scientific, and relevant information on disease states and Genentech medicines (Immunology/IBD).
  • Manage Phase I-III pediatrics and adult clinical trials in the assigned geographic area.
  • Support site identification, start-up, clinical trial recruitment, and study retention.
  • Ensure end-to-end customer experience by building and leveraging relationships with investigators, site staff, and clinical operations partners.
  • Engage with healthcare providers, clinical study staff, TAEs, population health decision makers, and patient thought leaders to further patient outcomes.
  • Identify educational gaps and provide insights on the IBD Disease Area to inform strategies.
  • Partner with cross-functional colleagues and global teams to develop and manage projects improving care for underserved populations.
  • Accountable for comprehensive activities for successful clinical development programs, including recruitment, competitive intelligence, Congress support, professional society engagement, and TA landscaping.
  • Cover multiple pipeline medicines and engage in clinical/scientific discussions to gather customer insights.
  • Serve as PoC for AI and Digital Strategies, leading initiatives on AI solutions and digital tools.

Benefits

  • Discretionary annual bonus may be available based on individual and Company performance.
  • Benefits detailed at the link provided below (https://roche.ehr.com/default.ashx?CLASSNAME=splash )
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