Genomics Clinical Laboratory Director Remote US
Imagine a world where you could detect health issues sooner to treat them more effectively.
Where food and water are always safe, even in remote corners of the earth.
And where scientific and medical research are enhanced to solve the greatest challenges of our times.
At PerkinElmer, we imagine this world every day.
Then, we innovate and collaborate to make it happen everywhere.
Our dedicated team of about 14,000 employees worldwide, pioneers scientific technologies for better detection, imaging, and informatics to help our customers work to create healthier families, improve the quality of life, and sustain the well-being and longevity of people globally.
If you are seeking a meaningful, impactful, and stimulating career, look no further.
PerkinElmer Genomics Clinical Laboratory DirectorProvides strategic leadership and direction for the delivery of enterprise-level support and service activities for company products and services.
Develops support delivery strategy and related processes, escalation procedures and training.
Liaises between customers and technical support, product development, sales and field service to identify opportunities for support delivery improvements, cost reduction and value-add to the customer/client.
Job DescriptionOVERVIEWWe are looking for an exceptional individual who is dual board certified in clinical cytogenetics and molecular genetics to perform clinical sign out,participate in development, validation and assay performance evaluation, and be the Medical Liaison and for ourvarious global sites for prenatal genomics services.
KEY FOCUS AREASLaboratory Testing:
Data management and reporting for Cytogenomic laboratory focusing on clinical diagnostic testing, client services, product validation.
Primarily responsible for reviewing, interpreting, and approving daily case load of clinical testing performed by the laboratory including reviewing and interpreting test results and reviewing, editing, and approving test reports.
Liaison between the clients and the laboratory, assist with questions about diagnostic testing.
Take a leading role in a focused testing area- CytogenomicsBe a part of the genome innovation team.
Travel to present scientific papers or market at scientific meeting(s)Other responsibilities include:
Evaluating and implementing new technologies and testing in the laboratoryValidating laboratory developed tests into clinical utilityAssuring test reports include pertinent and current information for test interpretationConsultation with case managers, genetic counselors, and laboratory staff concerning test results and the interpretation of those results as they relate to specific patient conditionsReviewing new test procedures, procedure manuals and assure that procedures are followed by personnelOngoing monitoring of each testing process used in the laboratory in order to identify errors or potential problems that could result in errors, taking corrective action and evaluating the corrective actions taken, to make sure that they were effective and will prevent recurrenceEvaluating the corrective actions taken, to make sure that they were effective and will prevent recurrenceParticipation in a CMS-approved proficiency testing (PT) program for all the tests performedRoutinely review quality control and quality assessment activities to assure problems occurring within the laboratory are identified and corrected and the corrections are monitored for effectiveness and timelinessBasic
Qualifications:
MD or PhD in a chemical, physical, biological, or clinical laboratory science.
ABMG-boarded certification in Clinical Cytogenetics and Molecular Genetics5+years'of experience in clinical molecular geneticsPreferred
Qualifications:
Prior experience desired in management of laboratory business including such areas as marketing, client services, total quality management, and technical service a definite plusDemonstrated success in technical proficiency, scientific creativity, collaboration with others and independent thought.
Ability to properly evaluate a wide variety of complex data from diverse laboratory, medical, and research sources and ability to integrate this information to provide a comprehensive, clinically relevant test petence in the following areas:
Write complex test reports and correspondence with internal and external clients.
Speak effectively before groups of customers or employees of organization.
Work with mathematical concepts such as probability and statistical inference.
Apply concepts such as fractions, percentages, ratios, and proportions to practical situations.
Define problems, collect data, establish facts, and draw valid conclusions.
Solve complex problems and deal with a variety of concrete variables in situations where only limited standardization terpret a variety of instructions furnished in written, oral, diagram, or schedule form.
Nothing in this job description restricts management's right to assign or reassign duties and responsibilities of this job at any time.
#LI-EXPDN-94946a57-07e7-4b9a-b9cb-1f50b1512fdb.
Estimated Salary: $20 to $28 per hour based on qualifications.
Where food and water are always safe, even in remote corners of the earth.
And where scientific and medical research are enhanced to solve the greatest challenges of our times.
At PerkinElmer, we imagine this world every day.
Then, we innovate and collaborate to make it happen everywhere.
Our dedicated team of about 14,000 employees worldwide, pioneers scientific technologies for better detection, imaging, and informatics to help our customers work to create healthier families, improve the quality of life, and sustain the well-being and longevity of people globally.
If you are seeking a meaningful, impactful, and stimulating career, look no further.
PerkinElmer Genomics Clinical Laboratory DirectorProvides strategic leadership and direction for the delivery of enterprise-level support and service activities for company products and services.
Develops support delivery strategy and related processes, escalation procedures and training.
Liaises between customers and technical support, product development, sales and field service to identify opportunities for support delivery improvements, cost reduction and value-add to the customer/client.
Job DescriptionOVERVIEWWe are looking for an exceptional individual who is dual board certified in clinical cytogenetics and molecular genetics to perform clinical sign out,participate in development, validation and assay performance evaluation, and be the Medical Liaison and for ourvarious global sites for prenatal genomics services.
KEY FOCUS AREASLaboratory Testing:
Data management and reporting for Cytogenomic laboratory focusing on clinical diagnostic testing, client services, product validation.
Primarily responsible for reviewing, interpreting, and approving daily case load of clinical testing performed by the laboratory including reviewing and interpreting test results and reviewing, editing, and approving test reports.
Liaison between the clients and the laboratory, assist with questions about diagnostic testing.
Take a leading role in a focused testing area- CytogenomicsBe a part of the genome innovation team.
Travel to present scientific papers or market at scientific meeting(s)Other responsibilities include:
Evaluating and implementing new technologies and testing in the laboratoryValidating laboratory developed tests into clinical utilityAssuring test reports include pertinent and current information for test interpretationConsultation with case managers, genetic counselors, and laboratory staff concerning test results and the interpretation of those results as they relate to specific patient conditionsReviewing new test procedures, procedure manuals and assure that procedures are followed by personnelOngoing monitoring of each testing process used in the laboratory in order to identify errors or potential problems that could result in errors, taking corrective action and evaluating the corrective actions taken, to make sure that they were effective and will prevent recurrenceEvaluating the corrective actions taken, to make sure that they were effective and will prevent recurrenceParticipation in a CMS-approved proficiency testing (PT) program for all the tests performedRoutinely review quality control and quality assessment activities to assure problems occurring within the laboratory are identified and corrected and the corrections are monitored for effectiveness and timelinessBasic
Qualifications:
MD or PhD in a chemical, physical, biological, or clinical laboratory science.
ABMG-boarded certification in Clinical Cytogenetics and Molecular Genetics5+years'of experience in clinical molecular geneticsPreferred
Qualifications:
Prior experience desired in management of laboratory business including such areas as marketing, client services, total quality management, and technical service a definite plusDemonstrated success in technical proficiency, scientific creativity, collaboration with others and independent thought.
Ability to properly evaluate a wide variety of complex data from diverse laboratory, medical, and research sources and ability to integrate this information to provide a comprehensive, clinically relevant test petence in the following areas:
Write complex test reports and correspondence with internal and external clients.
Speak effectively before groups of customers or employees of organization.
Work with mathematical concepts such as probability and statistical inference.
Apply concepts such as fractions, percentages, ratios, and proportions to practical situations.
Define problems, collect data, establish facts, and draw valid conclusions.
Solve complex problems and deal with a variety of concrete variables in situations where only limited standardization terpret a variety of instructions furnished in written, oral, diagram, or schedule form.
Nothing in this job description restricts management's right to assign or reassign duties and responsibilities of this job at any time.
#LI-EXPDN-94946a57-07e7-4b9a-b9cb-1f50b1512fdb.
Estimated Salary: $20 to $28 per hour based on qualifications.
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