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Clinical Operations Specialist III

Remote - US
USD $91,900~$114,800

We are looking for a Clinical Operations Specialist to support Invitae’s Clinical Information Team. The Clinical Information Team powers products and services across Invitae that help clients make informed medical decisions, including who to test and what to do with the result. We are responsible for structuring information within Invitae’s knowledge bases and ensuring products connect the right information to the right patient. This role will be responsible for content generation and curation of pre- and post-test genetic testing guidelines with implementation into Invitae’s products and systems. Additional responsibilities include utilization management, cross-functional collaboration, and participating in process improvement projects.

 

What you'll do: 

  • Evaluate primary literature for clinical guidelines and risk models that meet medical/legal/regulatory standards for inclusion in Invitae products
  • Create and enhance products utilizing curated clinical guidelines, including policies and risk models, that are tailored to the intended customer/product requirements.
  • Define clinical criteria that automates when an individual guideline or risk model is applied as output (this may involve building rules or mapping content to existing rules, depending on how the product rule engine is designed)
  • Test and validate accuracy of content and associated logic. Ensure consistency of clinical content amongst Invitae products.
  • Execute and structure all licensing requirements for content under copyright (e.g. NCCN) according to business needs. Provide ongoing clinical product and process support.
  • Collaborate with cross-functional teams. Provide stakeholder input to ensure no missed requirements.
  • Identifying improvements in existing processes and generating ideas for product development priorities

 

What you bring: 

  • Requires 5 years experience with Bachelor's degree, 3 year's experience with a Master's degree, and no experience with a PhD.
  • Preferred Master of Science or Master of Arts in Genetic Counseling granted by a genetic counseling program accredited by the American Board of Genetic Counseling (ABGC) or another health sciences degree
  • Preferred 2+ years of clinical and/or laboratory experience
  • Preferred experience in clinical cancer genetics
  • Professional knowledge of the rapidly changing principles and practice of medical, clinical, and laboratory genetics
  • Must have effective oral and written presentation and communication skills, superior organizational skills and be able to work independently

 

Please apply even if you don’t meet all of the “What you bring” requirements noted.  It’s rare that someone checks every single item, it’s ok, we encourage you to apply anyways.  

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