Senior Medical Science Liaison (East & West)

Clutch Canada

Carlsbad, CAFull-timePosted Apr 9, 2026

238K–251K a year

Behavioral Health Market Context

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Benefits

Paid Time OffDental CoverageHealth Insurance

Job Description

ical development, data generation, and pre-commercial readiness for dabogratinib and future pipeline programs.

This position requires a high degree of scientific expertise, autonomy, and executional focus, with direct investigator engagement, Key Opinion Leader (KOL) engagement, clinical trial support, and insights generation in a growing biotech environment. The Sr. MSL will serve as a key scientific partner to internal teams and external healthcare professionals.

Must have industry oncology experience as a Medical Science Liaison.
Key Job Responsibilities
• Lead and drive clinical trial and investigator support
• Proactively engage investigators and research staff in scientific discussions related to ongoing clinical trials, driving awareness and visibility of oncology programs
• Identify, develop, and maintain peer-to-peer scientific relationships with Key Opinion Leaders (KOLs) and healthcare professionals
• Collect, synthesize, and communicate actionable field insights to internal teams
• Identify emerging trends, competitive dynamics, and evolving standards of care in genitourinary oncology/urology
• Support scientific data dissemination and medical education initiatives
• Execute the scientific engagement plan
• Support Tyra’s presence at major oncology and urology congresses
• Maintain a high level of scientific expertise in oncology and urology
• Effectively collaborate with medical affairs, clinical development, clinical operations, and other cross-functional partners, ensuring alignment across programs
• Conduct all activities in accordance with regulations and company SOPs
• Facilitate problem-solving and conflict resolution with internal and external stakeholders to reduce issues / remove roadblocks and keep teams on track with key deliverables
• Proactively work with cross-functional teams to develop, progress, and accelerate program goals
• Serve as a role model within and outside of Medical Affairs in problem identification, cross functional collaboration, and implementation of planned resolutions
Education & Experience Required
• Advanced scientific degree required: MD, PharmD, or PhD
• Minimum 5+ years of MSL experience in oncology or urology (preferred) in the biotechnology or pharmaceutical industry, independently managing a large geographic territory
• Strong track record of supporting clinical trials in a late-stage or pre-commercial setting
• Late-stage oncology drug development (Phase 3) experience required, experience in bladder cancer a plus
• Proven track record of effectively networking and building new relationships
• Excellent communication and presentation skills
• Demonstrated success in advancing drug candidates to development
• Ability to provide technical advice and assist with problem resolution
• Prior experience working in a small, start-up biotech work environment preferred
• Strong analytical and strategic ability
• Ability to work independently and to multi-task
• Ability to change pace and tasks as needed and to work in a fast-paced environment
• Proficient in MS Outlook/Word/Excel/PowerPoint
• Must be able to travel extensively (~60-70%), primarily in the U.S. but also internationally as needed
Pay Range and Benefits

Base Salary Range: $238,467 - $250,800 USD

Individual compensation will be determined based on factors such as work location, skills, education, training, and experience.
What we offer US-based Employees:
• Competitive base, bonus, new hire and ongoing equity packages
• The starting compensation range(s) for this role is for a full-time employee (FTE) basis
• Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment
• Employer-paid Medical, dental, and vision insurance
• Employer-paid life insurance, AD&D, short-term disability, long-term disability, and EAP coverage
• 401(k) Plan with a fully vested company match 1:1 up to 4% of contributions
• Employee Stock Purchase Plan
• 14 -18 paid holidays, including office closure between December 25th and January 1st
• Flexible vacation
• Sick time
• Fitness Program
• Get Outdoors Program
• Paid parental leave benefit
• Tuition assistance

Job Type: Full-Time

Work authorization: United States (Required)

Work Location: Field

Equal Opportunity Employer: Tyra Biosciences, Inc. is an equal opportunity employer that is committed to providing a work environment free of harassment and discrimination based upon a protected category, as well as an environment free from retaliation for protected activity.

Qualifications

  • Must have industry oncology experience as a Medical Science Liaison
  • Advanced scientific degree required: MD, PharmD, or PhD
  • Strong track record of supporting clinical trials in a late-stage or pre-commercial setting
  • Proven track record of effectively networking and building new relationships
  • Excellent communication and presentation skills
  • Demonstrated success in advancing drug candidates to development
  • Ability to provide technical advice and assist with problem resolution
  • Strong analytical and strategic ability
  • Ability to work independently and to multi-task
  • Ability to change pace and tasks as needed and to work in a fast-paced environment
  • Proficient in MS Outlook/Word/Excel/PowerPoint
  • Must be able to travel extensively (~60-70%), primarily in the U.S. but also internationally as needed
  • Work authorization: United States (Required)

Benefits

  • Pay Range and Benefits
  • Base Salary Range: $238,467 - $250,800 USD
  • Individual compensation will be determined based on factors such as work location, skills, education, training, and experience
  • Competitive base, bonus, new hire and ongoing equity packages
  • The starting compensation range(s) for this role is for a full-time employee (FTE) basis
  • Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment
  • Employer-paid Medical, dental, and vision insurance
  • Employer-paid life insurance, AD&D, short-term disability, long-term disability, and EAP coverage
  • 401(k) Plan with a fully vested company match 1:1 up to 4% of contributions
  • Employee Stock Purchase Plan
  • 14 -18 paid holidays, including office closure between December 25th and January 1st
  • Flexible vacation
  • Sick time
  • Fitness Program
  • Get Outdoors Program
  • Paid parental leave benefit
  • Tuition assistance

Responsibilities

  • The MSL role is a field-based scientific expert responsible for establishing and advancing Tyra Biosciences’ medical presence in oncology, with a focus on urologic malignancies
  • This role will serve as a primary scientific interface between Tyra and the oncology/urology community, supporting clinical development, data generation, and pre-commercial readiness for dabogratinib and future pipeline programs
  • This position requires a high degree of scientific expertise, autonomy, and executional focus, with direct investigator engagement, Key Opinion Leader (KOL) engagement, clinical trial support, and insights generation in a growing biotech environment
  • MSL will serve as a key scientific partner to internal teams and external healthcare professionals
  • Lead and drive clinical trial and investigator support
  • Proactively engage investigators and research staff in scientific discussions related to ongoing clinical trials, driving awareness and visibility of oncology programs
  • Identify, develop, and maintain peer-to-peer scientific relationships with Key Opinion Leaders (KOLs) and healthcare professionals
  • Collect, synthesize, and communicate actionable field insights to internal teams
  • Identify emerging trends, competitive dynamics, and evolving standards of care in genitourinary oncology/urology
  • Support scientific data dissemination and medical education initiatives
  • Execute the scientific engagement plan
  • Support Tyra’s presence at major oncology and urology congresses
  • Maintain a high level of scientific expertise in oncology and urology
  • Effectively collaborate with medical affairs, clinical development, clinical operations, and other cross-functional partners, ensuring alignment across programs
  • Conduct all activities in accordance with regulations and company SOPs
  • Facilitate problem-solving and conflict resolution with internal and external stakeholders to reduce issues / remove roadblocks and keep teams on track with key deliverables
  • Proactively work with cross-functional teams to develop, progress, and accelerate program goals
  • Serve as a role model within and outside of Medical Affairs in problem identification, cross functional collaboration, and implementation of planned resolutions


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