A company is looking for an Assistant / Associate Clinical Director, Clinical Reporting.
Key Responsibilities :
Review and interpret clinical genomics data, ensuring accuracy in clinical laboratory reports
Partner with Quality Management to maintain compliance with regulatory guidelines and quality assurance standards
Identify opportunities for process improvement and collaborate on developing new laboratory tests and methodologies
Qualifications :
MD or Ph.D. in Clinical Laboratory Science, Genetics, Molecular Biology, or related field; ABMGG Board certified or eligible
Minimum of 2 years of relevant experience in a clinical laboratory setting
In-depth understanding of CLIA, CAP, and clinical laboratory operations regulatory requirements
Excellent analytical skills with a focus on interpreting laboratory data and quality control
Proficient in laboratory information systems (LIMS) and data analysis tools
Clinical Director Clinical Reporting • Fort Lauderdale, Florida, United States