Principal Clinical Molecular Geneticist

This is a fully remote position, open to applicants in Illinois.

📋 Description

• Analyze clinical genetic testing data and associated test reports.

• Address testing issues and review relevant scientific literature.

• Interpret genetic variants and compose/edit genetic test reports.

• Authorize laboratory test results for tests conducted.

• Curate gene panels utilizing extensive gene lists backed by scientific research.

• Coordinate and spearhead process enhancement projects aimed at cost reduction, efficiency, and productivity.

• Resolve technical issues and ensure corrective measures are implemented when systems diverge from laboratory standards.

• Act as a facilitator for exceptions and provide expertise for intricate cases.

• Engage in the selection of test methodologies and enhance systems, processes, and protocols.

• Mentor and develop team members.

• Foster communication, collaboration, employee growth, cross-functional teamwork, and conflict resolution.

• Communicate across various organizational levels and represent the company at conferences.

• Adhere to Standard Operating Procedures (SOPs), regulations, and Quality Management System policies.

• Uphold the company’s mission and values while maintaining consistent and reliable attendance.

⛳️ Requirements

• Doctoral Degree in Chemical, Biological, or Clinical Laboratory science from an accredited institution, along with necessary certification; or a Medical Doctor or Doctor of Osteopathic Medicine Degree with relevant clinical laboratory experience and pathology certification.

• Certification by the American Board of Bioanalysis (ABB) as a High-Complexity Clinical Laboratory Director (HCLD), or by the American Board of Medical Genetics and Genomics (ABMGG) in Laboratory Genetics and Genomics, Molecular Genetics, or Cytogenetics, or by the Canadian College of Medical Geneticists (CCMG); certifications must be obtained at hire and maintained throughout the duration of employment.

• A minimum of 3 years in a clinical laboratory with director oversight for the MD/DO pathway.

• Experience in conducting high complexity genetic testing.

• At least 4 years of post-certification experience in reviewing and signing out clinical test reports, or a total of over 7 years of experience in this area or equivalent.

• Valid New York State Certificate of Qualification in the necessary oversight areas, or the ability to acquire it within 6 months.

• Proven ability to fulfill essential duties with or without accommodation.

• Authorization to work in the United States without sponsorship.

• Capability to manage confidential information effectively.

• Proficient communication skills with employees, customers, healthcare providers, and vendors.

• Ability to thrive in a fast-paced, dynamic environment and contribute to project teams.

• Adherence to company SOPs, quality management policies, and relevant regulations.

• Willingness to work designated schedules, including nights and/or weekends as required.

• Competence in operating a mobile device, tablet, or computer and typing for approximately 90% of a standard working day.

• Readiness to travel up to 10% of working time, which may include overnight or weekend travel.

• Ability to approach work with an inclusive mindset.

🏝️ Benefits

• Opportunities for career advancement within an international company.

• Exceptional retirement savings plan featuring a substantial employer contribution.

• Company acknowledged as an excellent workplace in numerous countries globally.

• Recognized as one of the best large companies to work for, and among the top employers for diversity, working mothers, female executives, and scientists.