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Remote Anatomic Pathologist Jobs in Pennsylvania

Remote Anatomic Pathologist information

What is a remote anatomic pathologist?

A Remote Anatomic Pathologist is a medical doctor who specializes in diagnosing diseases by examining tissues and cells, but performs their work remotely using digital pathology platforms. They review high-resolution images of tissue samples sent electronically rather than working with physical slides in a laboratory. This allows them to provide diagnostic services, consultations, and second opinions from any location with secure internet access, improving access to pathology expertise and reducing turnaround times for results.

What are the key skills and qualifications needed to thrive as a remote anatomic pathologist?

To thrive as a Remote Anatomic Pathologist, you need a medical degree, board certification in pathology, and expertise in histopathological diagnosis. Familiarity with digital pathology platforms, laboratory information systems (LIS), and telepathology tools is crucial for efficient remote work. Strong attention to detail, effective communication, and time management skills help ensure accurate diagnoses and collaboration with clinical teams. These competencies are essential for delivering reliable pathology services remotely, supporting patient care, and maintaining diagnostic quality standards.

How does a remote anatomic pathologist collaborate with laboratory staff and clinicians when working off-site?

As a remote anatomic pathologist, collaboration with laboratory staff and clinicians is primarily achieved through secure digital platforms, video conferencing, and electronic medical records. You’ll regularly review digital slides, provide real-time or asynchronous consultations, and participate in virtual tumor boards or case discussions. Effective communication skills and familiarity with telepathology systems are essential, as you’ll need to ensure that your findings and recommendations are clearly conveyed to on-site teams for optimal patient care. Building strong working relationships remotely may take extra effort, but frequent updates and proactive communication help bridge the distance.

What is the difference between Remote Anatomic Pathologist vs Remote Clinical Pathologist?

AspectRemote Anatomic PathologistRemote Clinical Pathologist
CredentialsMedical degree, pathology residency, board certification in Anatomic PathologyMedical degree, pathology residency, board certification in Clinical Pathology
Work EnvironmentLaboratories, hospitals, diagnostic labs, often reviewing tissue samplesLaboratories, hospitals, diagnostic labs, analyzing blood, urine, and other clinical specimens
Employer & Industry UsageHospitals, pathology labs, academic institutionsHospitals, clinical labs, health systems
Search & Comparison IntentUnderstanding roles related to tissue diagnosis and histopathologyUnderstanding roles related to blood and bodily fluid analysis

Remote Anatomic Pathologists focus on diagnosing diseases through tissue and slide examination, while Remote Clinical Pathologists analyze blood, urine, and other clinical specimens. Both roles require similar medical credentials but differ in their work environment and diagnostic focus.

What are popular job titles related to Remote Anatomic Pathologist jobs in Pennsylvania?

For Remote Anatomic Pathologist jobs in Pennsylvania, the most frequently searched job titles are:

What cities in Pennsylvania are hiring for Remote Anatomic Pathologist jobs?

Cities in Pennsylvania with the most Remote Anatomic Pathologist job openings:

Clinical Pathologist II

Charles River Laboratories, Inc.

Horsham, PA • On-site, Remote

$180K - $200K/yr

Full-time

Medical, Retirement, PTO

Posted 17 days ago


Charles River Laboratories rating

8.4

Company rating: 8.4 out of 10

Based on 94 frontline employees who took The Breakroom Quiz

22nd of 86 rated pharmaceutical


Job description

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 occasional 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 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 120 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.


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About Charles River

Sourced by ZipRecruiter

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 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.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

Wilmington, MA, US

Year founded

1947