Review and interpret clinical genomics data, and sign out clinical laboratory reports, ensuring accuracy and reliability of clinical reporting.
Partner with Quality Management team on QC and QA programs to maintain the highest standards in laboratory testing and reporting, ensuring adherence to CLIA, CAP, and other regulatory guidelines.
Identify opportunities for process optimization, efficiency enhancement, and cost-effective laboratory practices.
Collaborate with Research & Development, bioinformatics and Genomic Technology team to develop, validate, and implement of new laboratory tests, methodologies, and data management and reporting systems.
Provide leadership and guidance to laboratory staff, including scientists, technicians, and support personnel.
Collaborate with cross-functional teams, including Lab Operation, Customer Service, Product, Commercial, to support company goals.

MD or Ph.D. in Clinical Laboratory Science, Genetics, Molecular Biology, or related field.
ABMGG Board certified or eligible in Clinical Molecular Genetics, Cytogenetics, or Laboratory Genetics and Genomics required.
Minimum of 2 years of relevant experience in a clinical laboratory setting.
In-depth understanding of CLIA, CAP, and other regulatory requirements pertaining to clinical laboratory operations.
Excellent analytical skills with a keen eye for detail, particularly in interpreting laboratory data and implementing quality control measures.
Effective verbal and written communication skills, ability to collaborate and interact with multidisciplinary teams.
Proven track record in identifying and resolving laboratory operational issues and challenges.
Proficient in laboratory information systems (LIMS), data analysis tools, and other laboratory-related software.

Associate Clinical Director, Clinical Reporting

Key skills