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Director, Pathologist

Employer
Labcorp
Location
Geneva, Switzerland
Salary
Competitive
Start date
19 May 2023
Closing date
18 Jun 2023

Job Details

The Director, Pathologist provides medical consultative and interpretive support to Labcorp Drug Development Central Laboratory Services and its internal and external customers. The iDirector, Pathologist will be responsible for medical decision-making and consultation that relate to laboratory services and clinical trials. Additional responsibilities include consulting with Quality Assurance, Safety Committee, Investigator Site Support, Project Management, Sponsors, and Investigators.

Duties and Responsibilities:

Laboratory Operations support:

  • Assist with the laboratory, medical or other company functions that require a pathologist, including analyses of and responses to medical or pathology/laboratory/clinical trials inquiries by customers.
  • Provide medical support and direction to the Laboratory Operations leaders.
  • Provide medical/pathology/clinical laboratory support to Laboratory operations departments and Investigators sites as needed.
  • Review of tissue slides for pathologist interpretation


Regulatory and Compliance:

  • As needed or requested, participate in investigator meetings, pathologist training for Companion diagnostic studies, or client visits to provide medical and laboratory support required for the success of a pharmaceutical drug clinical trial and submission of laboratory data to the FDA.
  • Consult with Quality Assurance to ensure compliance with applicable local and international regulations governing clinical reference laboratories, transport of clinical specimens, and pharmaceutical drug clinical trials.
  • Assist in interfacing with Sponsors and/or Regulatory authorities as needed.
  • Assist the site CAP Anatomic Pathology/Histology Certificate Holder, if necessary, in maintening the CAP laboratory accreditation requirements.


Scientific support:

  • Assist in the scientific professional growth of laboratory employees (provide guidance for professional development of staff, participates in interviews, makes hiring recommendations, leads disciplinary actions, delivers performance appraisal review, as required)
  • Collaborate with others in the organization in the creation and approval of reference ranges and appropriate test/method selection for a given clinical indication.
  • Advise in the development and approval of the technical database, the proprietary clinical trials database, and laboratory information systems.
  • Participate in the review and/or approval of new test or service feasibilities.
  • Pursue continuing or medical education in order to remain current in technology advances in the areas of laboratory medicine and clinical trials.
  • Contribute to scientific publications.


Business development and support:

  • As needed, interact with Sponsors and Medical Affairs group in protocol review and/or development
  • Perform literature review related to the therapeutic area involved in Sponsor clinical development
  • Communicate with clients' Project Managers to promote project schedule adherence within laboratory operations and meet high quality standards.
  • Make presentations and represent the company at professional meetings and with prospective and existing clients as required
  • Collaborate with business development in review, writing, presentation and defense proposals


Language Skills Required:
  • Speaking: French/English
  • Writing/Reading: French/English


Education/Qualifications:

Required:
  • This physician executive position requires a doctor of medicine degree with local licensure as applicable.
  • Certification in clinical pathology by the American Board of Pathology (IND) or European equivalent.
  • Excellent interpersonal skills and the ability to communicate comfortably with individuals at all levels from a multitude of educational, scientific, professional and national or international backgrounds.


Preferred:
  • Certification in anatomic pathology by the American Board of Pathology (IND) or European equivalent.


Experience:

Required:
  • Experience that satisfies the personnel requirement of CLIA 1988 or other applicable regulations for laboratory director.
  • Knowledge of clinical laboratory systems (testing, operations, finances, and information).


Labcorp is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, Labcorp strives for diversity and inclusion 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 of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), 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. We encourage all to apply.

For more information about how we collect and store your personal data, please see our Privacy Statement .

Company

At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions —because we know that knowledge has the potential to make life better for all. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations. Here, you can join our more than 70,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people’s lives. Join us in our pursuit of answers.

 

 

 

 

Company info
Website
Location
Maidenhead Office Park
Westacott Way
Littlewick Green
Maidenhead
SL6 3QH
United Kingdom

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