Senior Clinical Pathologist

Req ID #:  234188
Location: 

Ashland, OH, US, 44805

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.

Job Overview

BASIC SUMMARY:

Responsible for applying advanced scientific knowledge to interpret all aspects of clinical pathology conducted on research studies. Ensures customer satisfaction, scientific performance, and regulatory compliance, and oversees the scientific conduct of studies in the clinical pathology laboratory. Provides oversight and guidance to less experienced staff members.

 

ESSENTIAL DUTIES AND RESPONSIBILITIES:

  • Provides scientific oversight, ensure adherence to GLP regulations, and ensure quality of work by ensuring training, technical guidance, and review of data and reports are provided and by periodic review of processes.
  • Contributes to business development activities to include establishing and maintaining good client relations and representing clinical pathology to sponsors when required.
  • Provides scientific expertise and consultation for clinical pathology related issues to internal and external clients and serve as the point of contact for scientific issues related to departmental performance.
  • Responsible for preparation of assigned clinical pathology reports. Provides assistance to the Study Directors in the interpretation of clinical pathology endpoints and ensure that the data is accurately integrated into the final study report.
  • Performs testing facility management duties for the site as delegated by senior management
  • Provides scientific expertise for experimental design and conduct of research studies. Participates in method development. Participates in identification and evaluation of new instrumentation as required. Expands the array of assays to meet contemporary needs and expectations.
  • May serve as a study director or principal investigator.
  • Performs all functions required for management of direct report(s) and partners with Human Resources as needed for performance of these activities.
  • Functions as departmental representative for interdepartmental communications and initiatives as required
  • Attends scientific meetings, conferences, and training courses to enhance job and professional skills. Presents abstracts/posters at national meetings, when appropriate, to maintain a scientific presence and visibility in areas of individual expertise.
  • Directs the development of departmental training programs, as needed.
  • Performs all other related duties as assigned.

 

The salary for this position is a range of $185,000 - $247,000 annually. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

 

Job Description

MINIMUM QUALIFICATIONS:

  • Education: D.V.M. I V.M.D. (Doctor of Veterinary Medicine) degree or equivalent required.
  • Experience: A minimum of 6 years of pathology experience post-D.V.M.; working knowledge of clinical pathology, specialized training and/or experience in toxicologic pathology.
  • An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
  • Certification/Licensure: American College of Veterinary Pathologists (A.C.V.P.) board certification required. Experience may not be substituted for the board-certification at this level.
  • Other: Must have a reputation as an emerging leader in the company with sustained performance and accomplishment. Demonstrated success in technical proficiency, scientific creativity, collaboration with others and independent thought. Able to work on complex problems in which analysis of situations or data requires in-depth evaluation. Computer literacy in word processing, spreadsheet, and database software.
  • Must be authorized to work in United States without a sponsor visa now or in the future.

PREFERRED QUALIFICATIONS:

  • Ph.D. in Clinical Pathology or related discipline preferred.
  • American Board of Toxicology (A.B.T.) certification preferred.

WORKPLACE ENVIRONMENT:

  • Works in a laboratory environment with mild to moderate noise.
  • Potential exposure to chemical and/or biological hazards.
  • While performing the duties of this job the employee may occasionally be required to wear protective clothing (goggles, face shield, surgical mask, cap, gloves, scrubs, boots), and/or work near live animals with risk of exposure to allergens and/or zoonotic diseases.
  • The employee may occasionally be exposed to fumes or airborne particles, unpleasant odors, and/or wet, humid, and/or extreme temperature conditions.
  • While performing the duties of this job, the employee is regularly required to use a microscope and work/type at a computer.
  • Must be able to perform laboratory procedures, which require using appropriate instruments, reaching with hands and arms, working in narrow spaces.
  • Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus.

 

 

About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market.  Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.


About Charles River
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.

With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

We’re committed to providing benefits that elevate your quality of life.  Based on your position these may include:  bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.

 

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

 

For more information, please visit www.criver.com.


Nearest Major Market: Cleveland
Nearest Secondary Market: Mansfield

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