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Laboratory Director, Sign-Out

Lab

Pennsylvania

Remote

USD 168,000 - 200,000

Full time

Today
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Job summary

A leading genetic testing organization is seeking a Laboratory Director, Sign-Out for a remote position. Responsibilities include reviewing laboratory reports, providing clinical interpretations, and maintaining compliance in a high-throughput clinical laboratory setting. Candidates should have a PhD or MD along with ABMGG board certification in Clinical Molecular Genetics or LGG. This role offers a competitive salary range of $168,200-$200,000 and eligibility for bonuses.

Benefits

Comprehensive medical benefits
401(k) with company match
Tuition reimbursement
Employee Stock Purchase Plan
Flexible Time Off

Qualifications

  • ABMGG board certification in Clinical Molecular Genetics or LGG.
  • 3+ years of clinical laboratory director experience preferred.
  • Experience in a high-volume laboratory environment.

Responsibilities

  • Review and sign out laboratory reports.
  • Provide expert clinical interpretation.
  • Collaborate to support development and operations.

Skills

Strong technical background
Excellent communication skills
Ability to manage competing priorities
Collaboration skills
Patient care commitment

Education

PhD or MD or equivalent
ABMGG board certification
Licensed for high complexity testing
Job description

Labcorp Genetics (formerly Invitae) is dedicated to bringing comprehensive genetic information into mainstream medicine to improve healthcare for billions of people. Our team has a new opportunity for a Laboratory Director, Sign-Out. This remote, US based position will support high-throughput clinical laboratory reporting operations for molecular and microarray testing that is performed in the state-of-the-art San Francisco laboratory. Clinical areas of reporting focus for this team of laboratory directors include Women’s Health, Pediatrics and Rare Disease, and Hereditary Cancer. In addition to reporting, laboratory directors support laboratory operations, development efforts, change management, compliance and quality control, and troubleshooting. Individuals who are ABMGG (or equivalent) Board-certified in Clinical Molecular Genetics or LGG, or who have Active Candidate status (i.e., board-eligible in Clinical Molecular Genetics or LGG), are encouraged to apply.

Job Responsibilities

  • Review, interpret, and sign out laboratory reports in a range of clinical and technical areas
  • Provide expert clinical interpretation for atypical and abnormal clinical results
  • Maintain technical and clinical competency required to perform sign-out responsibilities
  • Work collaboratively in cross-functional settings to support operations, development, troubleshooting, and client inquiries
  • Participate in development and/or review of Standard Operating Procedures (SOPs) and Change Management
  • Serve as a stakeholder in incident response, quality affairs, change management, and medical policy
  • Provide clinical and/or technical expertise to support monitoring and improvement of current genetic tests, as well as development and launch of new test offerings
  • Provide consultation and/or communication to healthcare professionals and clients as needed
  • Serve as a positive representative of the team and organization, both internally and externally, in communication and professional interactions

Required Qualifications

  • PhD and/or MD degree OR equivalent (e.g., DO or DSc)
  • ABMGG board certification in Clinical Molecular Genetics or Laboratory Genetics and Genomics (LGG) OR Active Candidate Status (board eligible)
  • Licensed to perform high complexity testing or practice medicine in California OR eligible to obtain licensure (Clinical Genetic Molecular Biologist Scientist)
  • Strong technical and clinical background
  • Experience working in a high complexity CLIA/CAP laboratory
  • Knowledge of the regulatory requirements associated with a clinical laboratory
  • Excellent communication skills
  • Ability to attend to competing priorities in a positive and organized manner
  • Approachable and collaborative colleague and clinical professional
  • Commitment to exceptional patient care

Preferred Qualifications

  • 3+ years of clinical laboratory director experience
  • ABMGG board certification in Clinical Cytogenetics (in addition to ABMGG board certification in Clinical Molecular Genetics)
  • Licensed or eligible to obtain licensure in California for Clinical Cytogeneticist Scientist(in addition to Clinical Genetic Molecular Biologist Scientist)
  • New York State Certificate of Qualification, or eligibility, in relevant categories
  • Experience in a high-volume laboratory environment
  • Substantial prior experience in a broad range of clinical genetic testing modalities (e.g., NGS, WES, WGS, RNA, CMA)
  • Substantial prior experience in a broad range of clinical areas (e.g., Women’s Health, Pediatrics and Rare Disease, Oncology)

Application Window: 10/8-10/15

Pay Range: $168,200-$200,000

All job offers will be based on a candidate’s skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data.

The position is also eligible for an annual bonus under the Labcorp Bonus Plan. Bonuses are payable based on corporate and/or business segment performance and are subject to individual performance modifiers.

Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here.

Labcorp is proud to be an Equal Opportunity Employer:

Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.

We encourage all to apply

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