Senior Principal Scientist Veterinary Pathologist Board Certified
$231.9k - $365kMerck Sharp & Dohme (MSD)
Job DescriptionWe aspire to be the premier research-intensive biopharmaceutical company with over 130-year history. We’re at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. 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 varied pipeline of oncology, immunology, vaccines, biologics, small molecules, and newer modalities, we are at the forefront of research to advance the prevention and treatment of diseases such as cancer, cardiometabolic diseases, eye diseases, and infectious diseases.Our Company's Research Laboratories nonclinical drug safety department at West Point, Pennsylvania site is seeking an experienced anatomic pathologist to join a highly collaborative team of scientists (12 anatomic pathologists, 3 clinical pathologists, and approximately 40 exceptional laboratory scientists), working at a GLP-compliant facility with state-of-the-art anatomic, molecular and clinical pathology laboratories. This role is intended for an accomplished Pathologist with proven toxicological pathology and drug development experience with preferably immunology and biologics expertise who operates as a recognized subject‑matter expert and influences strategy from early discovery through late‑stage development. Our team works on a varied pipeline, participating in a wide variety of GLP-toxicology study types, many of which are run in-house, in addition to early discovery and investigative studies.Pathologists at our company are integral members and leaders of collaborative cross functional scientific teams, addressing challenges from early discoveries to late development. Our Company’s pathologists provide scientific leadership in the design and conduct of postmortem evaluation of studies and integrate the interpretation of postmortem data into the safety profile of drug candidates. Our Company's pathologists have a variety of opportunities to learn and grow as professional scientists and drug developers through daily study related activities and collaborative works with multiple program development teams. Key responsibilities for this scientific role include:Employ both routine H&E evaluations as well as other specialized techniques to characterize the safety profile of new drugs from toxicology and investigative studiesWork independently to analyze data, interpret and determine the significance of results for postmortem evaluations, review literature and design experiments to help teams solve scientific problems and advance programsDemonstrate scientific leadership with partnering broadly with toxicology, safety pharmacology, and translational teams to define mechanisms of toxicity, assess human relevance, and guide risk mitigation strategies for programs including immunology and biologics programs.Utilizing additional tools and applications that are all available on-site, including:An industry-leading suite of on-site in vitro and in vivo assay capabilitiesAccess to robust historical controls slide archive and data baseDigital PathologyTransmission electron microscopyImmunohistochemistry and in situ hybridizationQuantitative digital image analysis and targeted machine learning applicationsContribute to developing novel biomarkers and predictive models to de-risk drug candidates for safety-related liabilitiesOur Company's pathologists also serve as nonclinical drug safety department leads on drug development teams, overseeing the design and execution of studies, and generation of regulatory strategy and communications with global regulatory agencies to support the development of drug candidatesOur Company's pathologists work in a hybrid work environment and routinely interact with each other, share slides and opinions/experiences, and help each other learn and growRequired experience and skills:10+ years of experience as a veterinary pathologist7+ years of drug development experience in biotech, pharma, or CRO settingsLove to collaborate with diverse cross-functional teams and communicate openly and often with colleaguesDoctor of Veterinary Medicine (DVM)Residency in anatomic / toxicologic pathologyACVP, ECVP-board certification or equivalent in anatomic pathologyPreferred experience and skills:Strong knowledge of drug discovery, development and regulatory processes, including experience on drug development project teamsExperience in supporting immunology and biologics programsPhD in Immunology, Toxicology, Pathology, or related disciplineExperience serving as pathology lead for programs, or external due diligence as lead or subject matter expertise.Strong scientific leadership beyond individual studies, demonstrated growth and enterprise mindset, including cross-functional partnership, and cross ‑program influence and mentoring/management of other pathologists.Required Skills: Academic Research, Academic Research, Assay Development, Biopharmaceuticals, Biotechnology, Clinical Assays, Clinical Data Interpretation, Clinical Judgment, Clinical Safety, Collaborative Spirit, Detail-Oriented, Drug Development, Drug Discovery Research, Drug Research, Ethical Compliance, Exercises Judgment, Histopathology, Immunochemistry, Immunology Research, Innovation, In Vitro Research, In Vivo Models, Laboratory Processes, Molecular Diagnostic Techniques, Pathogenesis {+ 8 more}Preferred Skills: Current Employees apply HERECurrent Contingent Workers apply HEREUS 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 RightsEEOC GINA SupplementWe 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 ActsThe primary location for this posting is:USA - Pennsylvania - West PointWhere required by law, the compensation range for this role is provided below.The salary range for the primary location of this role is:$231,900.00 - $365,000.00This range reflects the Company's reasonable expectation of the base salary applicable to this role at the time of 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 .Additional location(s): Please note the salary range above applies to the Primary Location of the position. Where a role has other listed locations, different compensation guidelines may apply. You may find the salary ranges for additional locations below. If the salary range is not listed for the location you are applying to, our Talent Acquisition team will provide further information to you relevant to your location.Additional location(s) Compensation Information:San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance OrdinanceLos 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 OrdinanceSearch 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: RegularRelocation:Domestic/InternationalVISA Sponsorship:YesTravel Requirements:No Travel RequiredFlexible Work Arrangements:HybridShift:Not IndicatedValid Driving License:NoHazardous Material(s):N/AJob Posting End Date:11/14/2026*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. SummaryLocation: USA - Pennsylvania - West PointType: Full time
- ...Merck's Research Laboratories seeks an experienced veterinary pathologist to lead nonclinical drug safety assessments for oncology, immunology... ...development experience in biotech, pharma, or CRO ~ ACVP or ECVP board certification in anatomic pathology ~ Residency in...PrincipalSenior
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...Anatomic Pathologist We aspire to be the premier research-intensive... ...collaborative team of scientists (12 anatomic pathologists, 3... ...0+ years of experience as a veterinary pathologist ~7+ years of drug... ...toxicologic pathology ~ ACVP, ECVP-board certification or equivalent...PrincipalSeniorLocal areaRelocationVisa sponsorshipFlexible hoursShift work$282.2k
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...Research & Development Division in West Point, Pennsylvania, is seeking a dynamic and collaborative scientist for the Drug Metabolism and Pharmacokinetics (DMPK) group. The Principal Scientist will be a key contributor to multi-disciplinary drug development and discovery...PrincipalFull timeFor contractorsLocal areaFlexible hours- HireLifeScience in West Point, NY, is seeking an Associate Principal Scientist to join the Separations Sciences team. You will develop analytical methods to advance primarily the vaccines pipeline and collaborate with analytical/process project teams to deploy separation...Principal
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...vivo studies and integrate the findings from all contributing scientists into reports that characterize the safety profile of drug candidates... ...studies across all modalities. Interact with technical, veterinary, and scientific staff to ensure that the study is in compliance...SeniorFull timeContract workFor contractorsLocal areaFlexible hours
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