This job posting may have expired!
Use our `search` to find similar offers.
Similar jobs

Clinical Pathologist II

Charles River Laboratories International Inc (CRL)

Mattawan, MI, US, 49071

Job Summary

Job Summary:  A Clinical Pathologist 2 is 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, and give scientific input to laboratory staff and clients as requested. 

Essential Functions (The fundamental Duties & Responsibilities of the role (products and services provided/results accomplished) include, but are not limited to, those listed:    •    Responsible for preparation of assigned clinical pathology reports. Work with the Study Director to accurately integrate data into the final study report.  •    Responsible for the collection and reporting of clinical pathology data in studies. Provide assistance                to Study Directors in the interpretation of clinical pathology endpoints.  •    Serve as Study Clinical Pathologist, Study Director, or Principal Investigator on studies, as assigned, within the Clinical Pathology department.   •    Interact with Anatomic/Veterinary 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.  •    Conduct 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. 

Job Qualifications

Qualifications (Knowledge, Experience, Skills and Abilities required to accomplish the essential functions) include but are not limited to:  •    D.V.M. / V.M.D. (Doctor of Veterinary Medicine) degree required. Ph.D. in Clinical Pathology or related discipline preferred, with minimum 5 years of related experience in clinical pathology or experimental pathology.  •    Board certification by the American College of Veterinary Pathologists (D.A.C.V.P.) with specialty in Clinical Pathology required.  •    An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.  •    Demonstrated leadership skills as they pertain to intra- and interdepartmental initiatives, Sponsor interactions, and business development.  •    Ability to communicate verbally and in writing at all levels inside and outside the organization.  •    Basic familiarity with Microsoft Office Suite.  •    Computer skills, commensurate with Essential Functions, including the ability to learn a validated system.  •    Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.  •    Ability to work under specific time constraints. 

Compensation Data

The pay range for this position is $160,000-$170,000. 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 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 supported the development of 86% of the drugs approved by the FDA in 2021.

Equal Employment Opportunity

Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

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 [email protected]. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

Job posted: 2024-01-31

3
Abonnere