首席临床分子遗传学家
Principal Clinical Molecular Geneticist
艾博生物是全球医疗健康领域的领导者，帮助人们在生命各个阶段更好地生活。我们的产品组合涵盖各种改变生命的医疗技术，业务遍及诊断、医疗设备、营养品和品牌仿制药领域。我们的122,000名员工服务于全球160多个国家。
职位描述：
在艾博生物工作
在艾博生物，你可以从事有意义的工作，不断成长和学习，照顾自己和家人，做真实的自己，并过上充实的生活。你还将获得：
- 在一家国际公司中实现你梦想的职业发展机会。
- 一份雇主高比例出资的优秀退休储蓄计划。
- 一家被众多国家评为最佳工作场所的公司，并被《财富》杂志评为全球最受赞赏的公司之一。
- 一家被公认为最适合大公司工作的企业，同时也是最适合多样性、职场妈妈、女性高管和科学家工作的场所。
职位概述
高级临床分子遗传学家负责审查临床DNA检测数据和检测报告。该职位管理一组临床DNA测序检测，并在遗传病的一个子领域培养专业技能。高级临床分子遗传学家在遗传学家团队中担任思想领袖，指导流程改进并为复杂病例提供咨询。
主要职责
包括但不限于以下内容：
- 审查基因检测数据，必要时进行故障排查，查阅科学文献，解读基因变异，撰写或编辑基因检测报告，并对所执行的检测结果进行签发。
- 整理基因面板，包含由科学文献支持的全面基因列表。
- 协调并领导流程改进项目，以实现成本节约、效率提升和生产力提高。
- 在技术人员的帮助下排查技术问题，并确保当测试系统偏离实验室性能标准时采取纠正措施。
- 作为同事处理复杂病例的例外情况处理者和专家资源。
- 参与检测方法的选择，并主动改进系统、流程和程序，以提高日常生产的质量。
- 展示出开发和指导他人的能力。
- 通过促进沟通和协作来提供领导力。
查看英文原文
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,000 colleagues serve people in more than 160 countries.JOB DESCRIPTION:
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to:
- Career development with an international company where you can grow the career you dream of.
- An excellent retirement savings plan with a high employer contribution.
- A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.
- A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.
Position Overview
The Principal Clinical Molecular Geneticist reviews clinical DNA test data and test reports. This position maintains a Portfolio of clinical DNA sequencing tests and cultivates expertise in a subspecialty of genetic disease. The Principal Clinical Molecular Geneticist serves as a thought leader among the geneticist team, guiding process improvements and consulting on challenging cases.
Essential Duties
Include, but are not limited to, the following:
- Review genetic testing data, conduct troubleshooting when necessary, review the scientific literature, interpret genetic variants, write/edit genetic test reports, and sign out laboratory test results for tests performed.
- Curate gene panels to include comprehensive gene lists supported by scientific literature.
- Coordinate and lead process improvement projects to drive cost savings, efficiencies, and productivity.
- Troubleshoot technical problems, with the aid of technical staff, and ensure remedial action is taken whenever test systems deviate from the laboratory’s performance standards.
- Serve as an exception handler and expert resource for colleagues regarding complex cases.
- Participate in the selection of test methodology and take initiative to improve systems, processes, and procedures to drive quality in daily production.
- Demonstrate the ability to develop and coach others.
- Provide leadership by promoting communication and collaboration, proactively supporting employee development initiatives, promoting cross-functional collaboration and teamwork, and aiding in conflict resolution.
- Ability to manage confidential information.
- Effectively communicate cross-functionally to all levels within the company. Ability to establish and maintain effective working relationships by using appropriate interpersonal skills.
- Ability to frequently and accurately communicate with employees, customers, health care providers, and vendors, including representing the company at conferences.
- Thrive in a fast-paced, ever-changing environment and in project team situations.
- Comply with company Standard Operating Procedures (SOPs), practices, and applicable professional, Federal, State, and local regulations and assure that the laboratory is in compliance.
- Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork.
- Support and comply with the company’s Quality Management System policies and procedures.
- Maintain regular and reliable attendance.
- Ability to act with an inclusion mindset and model these behaviors for the organization.
- Ability to work designated schedule.
- Ability to work nights and/or weekends, as needed.
- Ability to work on a mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 90% of a typical working day.
- Ability to travel up to 10% of working time, which may include overnight/weekend travel.
Minimum Qualifications
- Must meet one of the following groups of criteria:
- Doctoral Degree in a Chemical, Biological, or Clinical Laboratory science from an accredited institution; and
- Certification by one of the following entities at the time of hire and maintained throughout employment; and:
- American Board of Bioanalytics (ABB) as a High-Complexity Clinical Laboratory Director (HCLD); or
- American Board of Medical Genetics and Genomics (ABMGG) in Laboratory Genetics and Genomics (LGG), Molecular Genetics, or Cytogenetics; or
- Canadian College of Medical Geneticists (CCMG).
- Medical Doctor or Doctor of Osteopathic Medicine Degree with 3+ years in a clinical lab with director oversight, certified in anatomical or clinical pathology, or both, by the American Board of Pathology or the American Osteopathic Board of Pathology at time of hire and maintained throughout employment in position.
- Years of experience performing high complexity genetic testing.
- 4+ years of post-certification experience reviewing and signing out clinical test reports; or
- 7+ years of total experience reviewing and signing out clinical test reports or equivalent.
- Current New York state Certificate of Qualification in appropriate areas of oversight as necessary or ability to obtain within 6 months.
- Demonstrated ability to perform the Essential Duties of the position with or without accommodation.
- Authorization to work in the United States without sponsorship.
The base pay for this position is
$113,300.00 – $226,700.00In specific locations, the pay range may vary from the range posted.
JOB FAMILY:
Research and DiscoveryDIVISION:
ONCO Cancer DiagnosticsLOCATION:
United States of America : RemoteADDITIONAL LOCATIONS:
WORK SHIFT:
StandardTRAVEL:
NoMEDICAL SURVEILLANCE:
NoSIGNIFICANT WORK ACTIVITIES:
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday)Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.EEO is the Law link - English: is the Law link - Espanol: Originally posted on Himalayas