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Tyra Biosciences

Develops precision oncology therapies targeting FGFR

VP – Medical Affairs

Biology & BiotechUpdated on Nov 10
Full-timeRemote in USA$405.7k - $442.6k

About the Job

Requirements

  • MD, PharmD, or PhD with extensive experience in Medical Affairs and Oncology.
  • 8–10+ years of experience in the pharmaceutical, biotechnology, or life sciences industry, with a strong background in global or US Medical Affairs.
  • Experience in genitourinary cancer; depth in bladder cancer is a significant plus.
  • A proven track record of leading medical strategies and teams in a complex, matrixed environment.
  • A strong understanding of clinical development, regulatory landscapes, and payer expectations in the US and/or major international markets.
  • Experience in launch planning, scientific engagement, and evidence generation in a highly competitive therapeutic area.
  • Deep expertise in medical communications, scientific publications, and external stakeholder engagement.
  • Excellent leadership skills and the ability to influence cross-functional teams and drive execution.
  • Direct contributions to high-impact publications and product launches.
  • Experience with the design and conduct of clinical trials and clinical operations.
  • The ability to create materials for internal and external audiences.
  • The ability to accommodate up to 20–30% travel or as business dictates.

Responsibilities

  • Develop and execute comprehensive medical affairs strategies aligned with corporate and commercial objectives.
  • Serve as the primary medical affairs leader overseeing scientific communications, medical education, key opinion leader engagement, real-world evidence generation, and medical insights.
  • Partner with R&D and Clinical Development teams to provide medical expertise on pipeline assets and shape evidence-generation plans.
  • Build and maintain relationships with key opinion leaders, healthcare professionals, and payers to drive scientific exchange and advocacy.
  • Represent the company at scientific congresses, advisory boards, and industry forums.
  • Provide scientific and medical leadership for investigator-initiated studies, post-marketing studies, and collaborative research initiatives.
  • Oversee the development and execution of medical education programs, advisory boards, and scientific symposia.
  • Lead publication planning and execution, ensuring high-quality scientific dissemination across medical journals and conferences.
  • Guide the development of medical and commercial materials, ensuring scientific accuracy and compliance with regulatory requirements.
  • Act as a bridge between Medical Affairs, Commercial, Market Access, and R&D teams to align product positioning and medical differentiation.
  • Partner with regulatory and legal teams to ensure medical activities comply with FDA, EMA, and other global regulatory requirements.
  • Provide leadership on initiatives supporting value demonstration and payer engagement.
  • Contribute to or lead process-improvement initiatives.
  • Perform other duties as assigned.

About the Company

Tyra Biosciences

Develops precision oncology therapies targeting FGFR

Tyra Biosciences develops precision medicines for cancer and genetically defined diseases using its SNAP platform to target specific genetic mutations. Its lead programs include TYRA-300, an FGFR3 inhibitor for achondroplasia and non-muscle invasive bladder cancer, and TYRA-200, an FGFR1/2/3 inhibitor for intrahepatic cholangiocarcinoma and other solid tumors. The SNAP platform supports mutation-focused drug design to overcome resistance and tailor therapies, aided by collaborations with academic partners to advance trials. Funding comes from venture capital and public offerings, with future revenue expected from drug sales and licensing upon regulatory approval, and the goal of bringing targeted, effective treatments to patients by moving candidates through clinical development toward commercialization.

Company size
51-200
Company stage
IPO
Headquarters
Carlsbad, CA
Founded
2018

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