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Principal Scientist, Veterinary Clinical Pathologist

Merck

Merck

West Point, PA, USA
USD 206,200-324,600 / year
Posted on Jun 10, 2025

Job Description

Principal Scientist (R5), Clinical Pathology, Pathology, Non-clinical Drug Safety, West Point

Our company is a leading global biopharmaceutical company with a long history of using the power of leading-edge science to save and improve lives around the world. Our success is driven by putting patients first, operating with the highest integrity, and committing fully to our vision to make a difference in the lives of people globally. With our diverse pipeline of vaccines, biologics, small molecules, and novel modalities, we are at the forefront of research to advance the prevention and treatment of diseases such as cardiometabolic, neurologic, immunologic, and infectious diseases as well as cancer.

About Us:

The Nonclinical Drug Safety organization at our Research Laboratories in West Point, Pennsylvania is seeking a veterinary clinical pathologist to join our highly collaborative Clinical Pathology group. This group is consisted of two ACVP-certified veterinary clinical pathologists and eleven laboratory-based scientific staff. You will work alongside an extensive Toxicology and Pathology team in a GLP-compliant facility equipped with state-of-the-art laboratories. Our team supports a diverse and exciting pipeline, supporting a wide variety of early discovery, investigative, and GLP-toxicity studies. Our clinical pathologists provide scientific leadership in study design and execution, as well as complete interpretations and reports for studies throughout drug development. Working collaboratively across the organization, these interpretations will offer a thorough analysis of clinical pathology data, including correlations to toxicokinetic data, antemortem evaluations, and histomorphologic findings for the program.

Key responsibilities for this scientific role include:

  • Review study protocol designs and make recommendations regarding clinical pathology portions of preclinical studies

  • Provide well-written, concise Clinical Pathology reports that accurately reflect the data collected and the significance/impact on candidate drug development and safety

  • Collaborate with Anatomic Pathologists and Toxicology Study Directors in the interpretation and communication of study results and provide the appropriate context of the data and its relevance to clinical development.

  • Serve as the nonclinical drug safety lead on drug discovery or development teams, overseeing the design and execution of studies, and providing critical regulatory strategy and communications with global regulatory agencies to support the development of drug candidates

  • Provide scientific leadership to the Clinical Pathology Lab group

  • Collaborate in novel biomarker development to support the pipeline

  • Actively engage in the external organizations to influence the regulatory environment for drug development.

Required educations, skills, and experience:

  • Experience collaborating with diverse cross-functional teams and communicating openly and often with colleagues

  • Doctor of Veterinary Medicine (DVM)

  • Residency in clinical pathology

  • ACVP-board certification in clinical pathology

  • MS or PhD in Toxicology, Pathology, or related discipline preferred but not required

  • 1-4 years of experience as a clinical pathologist in biotech, pharma or at a CRO is a plus, but not required

  • Excellent written and oral communication skills

Our company has a commitment to the continued professional development of all colleagues through training opportunities, publications, internal and external presentations, access to internal scientific seminars as well as support for external scientific meetings. With our location along the Northeastern US corridor, there are many opportunities to participate in cross-industry workshops, conferences, direct regulatory interactions and other training or networking opportunities. Imagine what you could achieve at our company!

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:

EEOC Know Your Rights

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We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.

Learn more about your rights, including under California, Colorado and other US State Acts

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Current Employees apply HERE

Current Contingent Workers apply HERE

US and Puerto Rico Residents Only:

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:

EEOC Know Your Rights

EEOC GINA Supplement​

We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.

Learn more about your rights, including under California, Colorado and other US State Acts

U.S. Hybrid Work Model

Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as “remote”.

The salary range for this role is

$206,200.00 - $324,600.00

This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.

The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.

You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.

San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance

Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status:

Regular

Relocation:

Domestic

VISA Sponsorship:

No

Travel Requirements:

No Travel Required

Flexible Work Arrangements:

Not Applicable

Shift:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

n/a

Required Skills:

Clinical Data Interpretation, Clinical Judgment, Clinical Pathology, Collaboration, Communication, Detail-Oriented, Drug Development, Ethical Compliance, Experimentation, Histopathology, Infectious Disease, Interpersonal Management, Mentoring Staff, Mentorship, Oral Communications, Pathology, Pathophysiology, Scientific Leadership, Social Collaboration, Teamwork, Toxicity Studies, Toxicology, Veterinary Medicine, Veterinary Pathology

Preferred Skills:

Job Posting End Date:

07/7/2025

*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.


Requisition ID:R352548