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.
The Physician Support Specialist Supervisor plays a key role in overseeing and coordinating the operational and quality initiatives within the medical practice, ensuring that all pre-analytical, analytical, and post-analytical processes align with the company's values and mission. This position is responsible for providing specialized support across various functions, ensuring quality control standards are met and maintained. The Physician Support Specialist Supervisor will collaborate with the medical team to streamline workflows and improve operational efficiency.
High School Diploma or equivalent required. Bachelor of Science degree, strongly preferred (chemical, physical, biological or clinical laboratory science or medical technology). Four (4) to seven (7) years of health care administration experience required. HT, HTL, or MT (ASCP) certification preferred. Experience in supervising teams or managing staff, with a proven ability to lead, guide, and mentor employees to achieve organizational objectives required. Knowledge of medical practice compliance. Experience with Quality Assurance and laboratory regulations/accreditation requirements preferred. Experience in all aspects of the AP laboratory operations desired. Other. Willingness to work overtime and at different shift times. Occasional travel will be required. Knowledge of CAP, CLIA, and state regulatory requirements such as New York State Department of Health.