Senior Medical Science Liaison

6 days ago

Toronto, Ontario, Canada AT Life Route Full time $50,000 - $125,000 per year

Senior Medical Science Liaison (MSL) – Neurology/Pediatrics (Texas/Oklahoma Region)

Location:
Hybrid – Texas or Oklahoma preferred

Travel:


50% required


Salary Range:
$200,000 – $250,000 USD annually

Work Authorization:
Must be authorized to work in the U.S.

Position Overview

The Senior MSL will play a pivotal role in educating healthcare professionals (HCPs) about Duchenne Muscular Dystrophy and investigational therapeutics within a growing product pipeline. Reporting to the West Region Team Leader, this role requires deep expertise in Neurology and/or Pediatrics, and a strong foundation in scientific communication and stakeholder engagement.

The ideal candidate is a driven, compassionate professional who thrives in a dynamic environment and is passionate about improving patient outcomes. This role also offers the opportunity to shape MSL processes, contribute to strategic planning, and support clinical development initiatives.

Key Responsibilities

  • Build and maintain collaborative relationships with key opinion leaders (KOLs), investigators, and institutions across academic, clinical, and healthcare settings.
  • Execute KOL engagement strategies, including identification, speaker development, and ongoing support.
  • Lead medical education efforts by delivering high-quality scientific presentations and facilitating data exchange with HCPs.
  • Represent Medical Affairs at scientific meetings, advisory boards, and investigator events.
  • Provide on-site support for clinical trials, investigator-initiated studies, and registries.
  • Assess potential clinical trial sites for capability and readiness.
  • Collaborate with internal teams to develop post-conference materials and gather competitive intelligence.
  • Stay current on Duchenne Muscular Dystrophy research and therapeutic advancements.
  • Support commercial teams with medical insights while maintaining compliance with regulatory standards.

Qualifications

  • Advanced degree (MD, PhD, PharmD, NP/PA preferred).
  • 5+ years of MSL experience strongly preferred.
  • Demonstrated compliance with industry and regulatory standards.
  • Proven ability to work independently and collaboratively.
  • Experience in Neurology and/or Pediatrics; immunology or gene therapy experience is a plus.
  • Strong understanding of clinical trial design and scientific data interpretation.
  • Excellent communication, presentation, and interpersonal skills.
  • High integrity, adaptability, and a proactive mindset.

Why Join Us?

We're seeking solution-oriented, critical thinkers who embrace ambiguity, value transparency, and lead with kindness and integrity. If you're passionate about making a difference in rare disease communities and thrive in a collaborative, fast-paced environment, we encourage you to apply.

Note:
This is a hybrid role. Occasional on-site work at company facilities and attendance at in-person events will be required.

Let me know if you'd like this tailored further for a specific audience (e.g., internal posting, LinkedIn, or a job board), or if you'd like help formatting it for a particular platform.

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