- Track NCCN, society, and other guidelines relevant to hereditary cancer risk assessment.
- Keep CancerIQ’s care pathways and risk models current and accurate, ensuring alignment with national standards.
- Be hands-on with customers and the platform:
- Update and validate care pathways and eligibility criteria, review edge cases, test product workflows, and join customer calls to provide clinical input.
- Lead research and publications:
- Define study questions, metrics, and cohorts; support IRB submissions; lead manuscript development; and co-author abstracts and papers with provider partners.
- Partner with Product & Engineering:
- Translate clinical workflows into product requirements.
- Validate rule logic and guideline automation
- Provide feedback on user experience to ensure accuracy and usability for frontline clinicians.
Requirements
- Background: Board-certified Genetic Counselor (CGC) or PhD in genetics, molecular biology, or a related field.
- Guidelines fluency: Deep familiarity with NCCN and other hereditary cancer guidelines and the ability to translate them into practical, clinical workflows.
- Hands-on mindset: Comfortable owning content end-to-end, from drafting eligibility criteria and care pathways to fielding customer questions and reviewing unusual patient cases.
- Research experience: Skilled in study design, IRB processes, data analysis, and scientific writing; published work is a plus.
- Tech comfort: Quick learner who can understand clinical software workflows, test logic, and provide actionable product feedback.
- Communication: Excellent written and verbal communicator who can make complex genetic concepts clear to both clinicians and non-clinical audiences.
- Teamwork: Collaborative, detail-oriented, and steady under pressure in a fast-moving, mission-driven environment.