Senior Staff Medical Science Liaison, Genetic Disease Testing, Reproductive Health

Illumina

. Serve as a field-based scientific resource and trusted scientific exchange partner for KOLs, healthcare professionals, laboratory personnel, researchers, academic institutions, and other stakeholders .

Posted 10/5/2026full-timeRemote • United StatesSenior💰 $155,600 - $233,400 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in genomics, molecular diagnostics, and translational research, with a strong ability to communicate complex scientific data effectively to diverse audiences. Proven experience in building collaborative relationships and ensuring compliance with industry regulations and ethical standards.

Highest-signal resume keywords

Advanced Degree In Relevant Scientific DisciplineClinical Laboratory ExperienceUnderstanding Of Genomics And Personalized MedicineMSL Experience In GenomicsThorough Understanding Of FDA, CLIA, And HIPAA Regulations

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Genomic TechnologiesTranslational ResearchMolecular DiagnosticsClinical Laboratory WorkflowsScientific Data InterpretationEvidence-Based Scientific EducationAnalytic SkillsPublication PlanningResearch And Publication RecordCompliance Knowledge

Soft Skills

Problem-SolvingAnalytical ThinkingCommunication SkillsRelationship BuildingCollaboration

Certifications & Qualifications

Certified Genetic Counselor

Industry Keywords

Medical Device IndustryClinical ResearchIn Vitro DiagnosticsMedical AffairsStakeholder Engagement

About the role

Key responsibilities & impact

Serve as a field-based scientific resource and trusted scientific exchange partner for KOLs, healthcare professionals, laboratory personnel, researchers, academic institutions, and other stakeholders
Conduct factual, objective, non-promotional scientific interactions in accordance with company policies and practices
Develop and maintain expertise in genomic technologies, translational research, emerging scientific evidence, and molecular diagnostics relevant to genetic disease and reproductive health
Monitor key publications, scientific trends, and evolving standards affecting genomics
Build collaborative relationships with external scientific leaders and stakeholders
Deliver objective, balanced, evidence-based scientific education on genomics, precision medicine, and emerging research
Collect, analyze, and communicate stakeholder insights to inform Medical Affairs strategy, evidence generation, education, and research priorities
Support scientific exchange at congresses, advisory boards, investigator meetings, and research-focused forums
Respond to unsolicited requests for scientific information about Illumina products and technologies
Facilitate dissemination of approved scientific information and materials
Provide scientific support for investigator-sponsored, collaborative, Illumina-sponsored clinical, and research studies
Partner cross-functionally with Research & Development, Product Management, Regulatory Affairs, Market Access, Legal, Compliance, and Commercial teams
Contribute to publication planning, scientific communications, evidence dissemination, and external scientific content review
Maintain Medical Affairs independence and compliance with applicable regulations, industry guidance, company policies, and ethical standards

Requirements

What you’ll need

Advanced degree required in a relevant scientific discipline (MS/certified genetic counselor or PhD)
Clinical laboratory experience strongly preferred
Strong understanding of and experience interacting with compliance, legal, product management, commercial teams, and other relevant functions in the medical device industry
Understanding of genomics, personalized medicine, in vitro diagnostics, clinical laboratory workflows, and genetics background with a research and publication record preferred
Greater than or equal to 5 years of clinical, scientific/research, or industry-related experience or equivalent required
Ability to interpret scientific data, understand its potential impact on clinical practices and research needs, and communicate scientific data to broad audiences
Thorough understanding of FDA, CLIA, HIPAA, and laws and regulations relevant to the medical device industry
Advanced problem-solving and analytic skills
At least 3 years of MSL experience or equivalent in genomics
More than 5 years preferred
Must be willing to travel 50% of the time

Benefits

Comp & perks

Variable cash programs (bonus or commission)
Equity for eligible roles
Access to genomics sequencing
Family planning
Health, dental, and vision benefits
Retirement benefits
Paid time off
Employee Resource Groups offering career development experiences, cultural awareness, and social responsibility opportunities