Everly Health's mission is to transform lives with modern, diagnostics-driven care, and we believe that the future of healthcare is meeting people where they are. Headquartered in Austin, Texas, Everly Health is the parent company to Everlywell, Everly Health Solutions, Natalist, and Everly Diagnostics. We've set a new standard of people-focused, diagnostic-driven care that puts patients at the center of their own health journey.
Our infrastructure guides the full testing experience with the support of a national clinician network that's composed of hundreds of physicians, nurses, genetic counselors, PharmDs, and member care specialists. Our solutions make world-class virtual care more attainable with rigorous clinical protocols and best-in-class science to tackle some of the healthcare industry's biggest problems.
The R&D Scientist will serve as an active member of the clinical lab and provide scientific support to ongoing method/assay development and validation. This includes generation of pre-protocol documentation (development/validation plans), conduct experiments, review results and provide a report on results and conclusions.
Responsibilities:Apply the principles, theory and techniques of Good Laboratory Practices to produce and report appropriate clinical lab resultsMonitor test analyses and specimen examinations to ensure that acceptable levels of analytic performance are maintained.Development of new tests/assays and/or improvement of existing tests Implementation of new/improved tests in the clinical laboratory providing training to clinical lab personnelPerform preventative and corrective maintenance on instrumentation as prescribed in procedures and/or as described by manufacturer specifications.Review and analyze statistical analysis plans and data setsAble to review literature and competitive information for clinical trial design planning and analysis of resultsCollaborate with various groups for study level publication planning including manuscript writing and submissionsCollaborate to achieve publications for clinical study data through coordination with investigator authors and project management of reviews and revisions for abstracts and manuscriptsGenerate documents to support regulatory submissions Record corrective action when necessaryRequired Skills/Experience:Knowledge of small molecules LC-MS/MS (method development and validation)PhD with a minimum of 1 year of experience in a Clinical LaboratoryOr Masters Degree with 2 years of experience in a Clinical LaboratoryOr Bachelors Degree and/or MLT or MLS with 4 years of experience in Clinical LaboratoryExperience conducting research or testing on human specimens in a Clinical Laboratory across multiple areas (Chemistry, Special Chemistry, Molecular, Microbiology)Experience and strong knowledge of data analysis and interpretation skillsStrong verbal and written communication skills and interpersonal skills.Strong leadership skills as it will require significant interaction with executive leadership, physicians, and regulatory authorities.Estimated Salary range:
Our salary intelligence, powered by our AI algorithms, has calculated an estimated range for this position between $70,000 - $90,000 . Please note that the actual salary for this position may vary, as it is dependent on various factors including but not limited to experience, location, and market dynamics.
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