Clinical Pathologist II

At Charles River, we are passionate about improving the quality of people's lives. When you join our global family, you will help create healthier lives for millions of patients and their families.

Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career.

As a Charles River employee, you will be part of an industry-leading, customer-focused company at the forefront of drug development. Your skills will play a key role in bringing life-saving therapies to market faster through simpler, quicker, and more digitalized processes. Whether you are in lab operations, finance, IT, sales, or another area, when you work at Charles River, you will be the difference every day for patients across the globe.

** Job Overview*
* Responsible for all aspects of clinical pathology conducted on research studies. Partner with Study Directors to provide comprehensive interpretation and preparation of the clinical pathology portions of reports. Participate in protocol development, measurement of hematology, coagulation, clinical chemistry, and urinanalytical parameters.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

+ Responsible for the interpretation of clinical pathology data and preparation of comprehensive clinical pathology reports. Aid Study Directors in the interpretation of clinical pathology endpoints.

+ Serve as Study Clinical Pathologist or Principal Investigator on studies, as assigned within the Clinical Pathology department, including in situ hybridization and immunohistochemistry.

+ Interact with Anatomic Pathologists to ensure relevant and appropriate correlations for clinical and anatomical pathology endpoints.

+ Evaluate study specimens related to clinical pathology, such as blood smears, bone marrow smears, urinalysis sediment preparations and body fluid preparations. Evaluate other materials as necessary and appropriate.

+ Provide scientific expertise for experimental design and conduct of research studies. Participate in method development, and identification and evaluation of new instrumentation, as required. Assist in expanding the array of clinical pathology assays to meet contemporary needs and expectations.

+ Assist in on-site employee training in clinical pathology or related topics as needed for studies, specialty projects or continuing education.

+ Provide expertise and guidance to Clinical Pathology personnel with technical issues.

+ Review and approve new/revised Standard Operating Procedures (SOPs) pertaining to pathology. Confirm department SOPs are developed and maintained according to established guidelines.

+ Interact and communicate with Sponsors as needed to ensure good client relations.

+ Participate on committees and in professional activities as deemed appropriate.

+ Perform all other related duties as assigned.

Note:

+ This position is open to a Hybrid or Remote work schedule.

+ This position will require some occassional travel.

** Job Qualifications*
* +

Education:

DVM/VMD (Doctor of Veterinary Medicine) degree or equivalent required. Ph.D. in Clinical Pathology or related discipline preferred.

+

Experience:

Minimum 3 years related experience in clinical pathology or experimental pathology with demonstrated research capability as demonstrated by publications in peer-reviewed journals. Experience in the contract research or pharmaceutical industry with Postdoctoral experience or advanced/specialized education preferred. .

+ An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.

+ Certification/Licensure:
Board certification by the American College of Veterinary Pathologists (D.A.C.V.P.) Specialty in Clinical Pathology required.

+ Other:
Full understanding of regulatory requirements, Good Laboratory Practices (GLPs), site SOPs, and of study types assigned. Knowledge of applicable international guidelines for all types of toxicology studies. Demonstrate leadership skills as they pertain to intra- and interdepartmental initiatives, Sponsor interactions, and business development. Effective written and verbal communication skills. Ability to handle multiple projects, prioritize work and meet deadlines. Proficiency in the use of standard software including Microsoft® Excel, Word, PowerPoint, etc.

and with standard laboratory calculations and statistical interpretation.

** Compensation Data*
* The pay range for this position is $180,000 - $200,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

** 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…