Fulgent Genetics
Job Details
Experienced IDX Phoenix AZ Site - PHOENIX, AZ Full Time Graduate Degree Health Care
About Us Inform Diagnostics, a Fulgent Genetics Company, is a nationally recognized diagnostics laboratory focused on anatomic pathology subspecialties including gastrointestinal pathology, dermatopathology, urologic pathology, hematopathology, and breast pathology. Founded in 2011, our parent entity, Fulgent Genetics, has evolved into a premier, full-service genomic testing company built around a foundational technology platform. Through our diverse testing menu, Fulgent is focused on transforming patient care in oncology, anatomic pathology, infectious and rare diseases, and reproductive health. We believe that by providing a wide range of effective, flexible testing options in conjunction with best‑in‑class service and support, we can redefine the way medicine is managed for patients and clinicians alike. Since integrating with our therapeutic development business, Fulgent is also developing drug candidates for treating a broad range of cancers using a novel nanoencapsulation and targeted therapy platform. By merging our fields of expertise, we aim to become a fully integrated precision medicine company.
Summary of Position Primarily responsible for review and sign out of flow cytometry, bone marrow, and morphology cases. Also responsible for reviewing and signing out of surgical pathology cases as needed.
Key Job Elements
Responsible for review and sign‑out of hematopathology cases in the areas of flow cytometry, FISH, molecular, and bone marrow/tissue consultation.
Responsible for reviewing and signing out of surgical pathology consultation cases, including FISH and molecular cases.
Application of accepted criteria in formulating and reporting diagnostic information on various anatomic hematopathology specimens.
Diagnostic interpretation of specimens processed within the laboratory.
Ensure that the reports of test results include pertinent information required for interpretation.
Ordering/interpretation of appropriate immunohistochemical stains and special stains.
Interpretation/sign‑out of pathology specimens within CAP guidelines for turnaround time.
Provide clinical laboratory consultation to technical personnel and healthcare providers.
Participation in Quality Assurance measures for the laboratory as required by accreditation standards.
Provide residents and/or trainees with information on specimen evaluation and reporting as needed.
Provide on‑call services as designated in the department schedule.
Perform other responsibilities as requested or required by CLIA and other local, state, or federal regulations.
Qualifications Knowledge/Experience
Minimum of five years related clinical experience in a laboratory setting.
Doctor of Medicine (MD).
Certified in Hematopathology and Anatomic Pathology (AP) and/or Anatomic and Clinical Pathology (AP/CP), by the American Board of Pathology or possess equivalent qualifications.
Laboratory personnel participating in licensure or certification maintenance programs must complete the number of continuing education hours prescribed by their licensing or certifying agency.
Technical laboratory personnel whose certification has been grandfathered and does not require participation in a certification maintenance program must complete at least twelve hours of continuing education annually.
Possess a current license as issued by the Georgia Composite Medical Board.
Environment Fulgent Therapeutics LLC is an Equal Employment Opportunity Employer. The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions. The term “qualified individual with a disability” means an individual with a disability who, with or without reasonable accommodation, can perform the essential functions of the position.
Seniority Level Mid‑Senior level
Employment Type Full‑time
Job Function Health Care Provider
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About Us Inform Diagnostics, a Fulgent Genetics Company, is a nationally recognized diagnostics laboratory focused on anatomic pathology subspecialties including gastrointestinal pathology, dermatopathology, urologic pathology, hematopathology, and breast pathology. Founded in 2011, our parent entity, Fulgent Genetics, has evolved into a premier, full-service genomic testing company built around a foundational technology platform. Through our diverse testing menu, Fulgent is focused on transforming patient care in oncology, anatomic pathology, infectious and rare diseases, and reproductive health. We believe that by providing a wide range of effective, flexible testing options in conjunction with best‑in‑class service and support, we can redefine the way medicine is managed for patients and clinicians alike. Since integrating with our therapeutic development business, Fulgent is also developing drug candidates for treating a broad range of cancers using a novel nanoencapsulation and targeted therapy platform. By merging our fields of expertise, we aim to become a fully integrated precision medicine company.
Summary of Position Primarily responsible for review and sign out of flow cytometry, bone marrow, and morphology cases. Also responsible for reviewing and signing out of surgical pathology cases as needed.
Key Job Elements
Responsible for review and sign‑out of hematopathology cases in the areas of flow cytometry, FISH, molecular, and bone marrow/tissue consultation.
Responsible for reviewing and signing out of surgical pathology consultation cases, including FISH and molecular cases.
Application of accepted criteria in formulating and reporting diagnostic information on various anatomic hematopathology specimens.
Diagnostic interpretation of specimens processed within the laboratory.
Ensure that the reports of test results include pertinent information required for interpretation.
Ordering/interpretation of appropriate immunohistochemical stains and special stains.
Interpretation/sign‑out of pathology specimens within CAP guidelines for turnaround time.
Provide clinical laboratory consultation to technical personnel and healthcare providers.
Participation in Quality Assurance measures for the laboratory as required by accreditation standards.
Provide residents and/or trainees with information on specimen evaluation and reporting as needed.
Provide on‑call services as designated in the department schedule.
Perform other responsibilities as requested or required by CLIA and other local, state, or federal regulations.
Qualifications Knowledge/Experience
Minimum of five years related clinical experience in a laboratory setting.
Doctor of Medicine (MD).
Certified in Hematopathology and Anatomic Pathology (AP) and/or Anatomic and Clinical Pathology (AP/CP), by the American Board of Pathology or possess equivalent qualifications.
Laboratory personnel participating in licensure or certification maintenance programs must complete the number of continuing education hours prescribed by their licensing or certifying agency.
Technical laboratory personnel whose certification has been grandfathered and does not require participation in a certification maintenance program must complete at least twelve hours of continuing education annually.
Possess a current license as issued by the Georgia Composite Medical Board.
Environment Fulgent Therapeutics LLC is an Equal Employment Opportunity Employer. The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions. The term “qualified individual with a disability” means an individual with a disability who, with or without reasonable accommodation, can perform the essential functions of the position.
Seniority Level Mid‑Senior level
Employment Type Full‑time
Job Function Health Care Provider
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