Sr Staff Medical Affairs Specialist (Genomics)

Location: US - Remote

Base salary: $155,600–$233,400 per year, plus eligible bonus or commission and potential equity.

Company

hirify.global develops genomic technology that supports early disease detection, diagnosis, treatment options, and broader health equity.

What you will do

• Review scientific, medical, and promotional materials through the Content Approval Process, ensuring accuracy, appropriate evidence, balanced messaging, and compliance.
• Provide medical and scientific guidance to Marketing, Commercial, Regulatory, Legal, Compliance, and other stakeholders.
• Lead the development and continuous improvement of Medical Affairs review processes, SOPs, work instructions, and governance frameworks.
• Partner with global, regional, and segment-specific Medical Affairs teams on strategic initiatives and compliant communications.
• Drive process improvements, operational excellence, and timely execution in a global matrix environment.

Requirements

• Advanced degree in life sciences, such as a PhD, MS, certified genetic counselor qualification, or equivalent.
• At least 8 years of relevant industry experience in Medical Affairs, Medical Information, Scientific Communications, Medical Review, Clinical Affairs, Regulatory Affairs, or a related function.
• Expertise in reviewing scientific, medical, and promotional materials and applying healthcare regulations, industry codes, and compliance requirements.
• Experience with Medical Affairs governance, content approval processes, quality systems, document lifecycle management, SOPs, and work instructions.
• Strong scientific judgment, analytical ability, communication skills, stakeholder influence, and project management experience.
• Ability to work independently, provide training and mentorship, and balance scientific integrity, compliance, efficiency, and business objectives.

Nice to have

• Genetic counselor experience.
• Experience with CAP, PRC, MRC, or similar formal review frameworks.
• Knowledge of diagnostic, genomics, molecular testing, biotechnology, medical device, or pharmaceutical regulations and standards.
• Experience with content management, approval workflow, document control, global process harmonization, inspection readiness, or quality initiatives.

Culture & Benefits

• Full-time employment in a remote US role.
• Health, dental, and vision coverage, retirement benefits, paid time off, and family planning support.
• Access to genomics sequencing benefits and employee resource groups supporting development, cultural awareness, and social responsibility.
• Inclusive workplace focused on collaboration, belonging, and equal opportunity.
• Visa sponsorship is not available for this role.