
Senior Staff Medical Science Liaison, Genetic Disease Testing, Reproductive Health
Posted Oct 6

Posted Oct 6
This is a fully remote position, open to applicants in United States.
• Act as a field-based scientific resource and a reliable partner for scientific exchange with KOLs, healthcare professionals, laboratory staff, researchers, academic institutions, and other stakeholders.
• Engage in factual, objective, and non-promotional scientific interactions in line with company policies and practices.
• Cultivate and sustain expertise in genomic technologies, translational research, emerging scientific evidence, and molecular diagnostics pertinent to genetic diseases and reproductive health.
• Keep abreast of key publications, scientific developments, and changing standards impacting genomics.
• Establish collaborative relationships with external scientific leaders and stakeholders.
• Provide objective, balanced, and evidence-based scientific education on genomics, precision medicine, and cutting-edge research.
• Gather, analyze, and convey stakeholder insights to guide Medical Affairs strategy, evidence generation, education, and research priorities.
• Facilitate scientific exchange at congresses, advisory board meetings, investigator meetings, and research-focused forums.
• Address unsolicited inquiries for scientific information regarding Illumina products and technologies.
• Aid in the dissemination of approved scientific information and materials.
• Offer scientific support for investigator-sponsored, collaborative, and Illumina-sponsored clinical and research studies.
• Collaborate across functions with Research & Development, Product Management, Regulatory Affairs, Market Access, Legal, Compliance, and Commercial teams.
• Contribute to publication planning, scientific communications, evidence dissemination, and the review of external scientific content.
• Uphold the independence of Medical Affairs while ensuring compliance with applicable regulations, industry guidelines, company policies, and ethical standards.
• An advanced degree in a relevant scientific discipline is required (MS/certified genetic counselor or PhD).
• Clinical laboratory experience is highly preferred.
• Strong knowledge and experience with compliance, legal, product management, commercial teams, and other pertinent functions within the medical device industry.
• Familiarity with genomics, personalized medicine, in vitro diagnostics, clinical laboratory workflows, and a genetics background with a research and publication record is preferred.
• Minimum of 5 years of clinical, scientific/research, or industry-related experience, or equivalent, is required.
• Ability to interpret scientific data, grasp its potential impact on clinical practices and research needs, and effectively communicate scientific data to diverse audiences.
• Comprehensive understanding of FDA, CLIA, HIPAA, and other laws and regulations applicable to the medical device industry.
• Advanced problem-solving and analytical capabilities.
• At least 3 years of MSL experience or equivalent in genomics, with a preference for more than 5 years.
• Willingness to travel 50% of the time is required.
• Variable cash programs (bonus or commission).
• Equity options for eligible positions.
• Access to genomic sequencing.
• Family planning assistance.
• Comprehensive health, dental, and vision benefits.
• Retirement benefits.
• Paid time off.
• Participation in Employee Resource Groups that offer career development experiences, cultural awareness, and opportunities for social responsibility.
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