Scientific Director, Clinical Pathology

We need to output HTML fragment with sections: About the role? The posting includes Position Summary, Key Responsibilities, Qualifications, Compensation Overview, Benefits, How We Work, Supporting People With Disabilities, Candidate Rights, Data Protection. But we must only include sections when posting has real, specific content. We should not include headings with filler like "commensurate with experience". We need to use

for section headings (e.g., About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule). However we can use other headings? The instruction says: use

for section headings (e.g. About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule). It suggests we should use those headings if appropriate. But we can also use other headings? Likely they want us to map content to those standard headings. For example: Position Summary could be "About the role". Key Responsibilities -> "Responsibilities". Qualifications -> "Qualifications". Compensation Overview -> "Pay". Benefits -> "Benefits". How We Work maybe could be "Schedule"? Not exactly; schedule refers to work schedule. Could be omitted if not specific. Supporting People With Disabilities etc are EEO/legal boilerplate; we should remove cookie/navigation/legal/EEO/equal-opportunity/scam-warning boilerplate, duplicated lines, and application instructions. So we should drop Supporting People With Disabilities, Candidate Rights, Data Protection, etc. Also "How We Work" maybe not boilerplate but could be considered generic; but it's about work models. Might be considered relevant but not a standard heading; maybe we could include as a paragraph under About the role? The instruction says prefer a few substantive sections over many thin ones. So we could combine some. We must preserve ALL substantive information; do not invent or summarize away detail. So we need to keep the details from Position Summary, Key Responsibilities, Qualifications, Compensation Overview, Benefits. Also maybe the "We hire for skills..." statement is part of Qualifications? It's a note encouraging apply; could be included in Qualifications or as a separate note but we can keep within Qualifications. We must not repeat the job title as a heading. The job title is "Scientific Director, Clinical Pathology" (from the end). So we should not put that as heading. We must not put Job ID/requisition numbers as headings; we can drop them. We need to output only HTML fragment, no /, no markdown fences. Thus produce something like:

About the role

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it. Position Summary BMS is seeking a veterinary Clinical Pathologist to join a large and well-established biopharmaceutical company dedicated to developing safe and efficacious medicines for areas of unmet need. This is an exciting opportunity to work within a highly experienced, collaborative, and supportive group of pathologists, where career growth is actively encouraged.

But we need to avoid duplication; maybe combine. Better:

About the role

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it. BMS is seeking a veterinary Clinical Pathologist to join a large and well-established biopharmaceutical company dedicated to developing safe and efficacious medicines for areas of unmet need. This is an exciting opportunity to work within a highly experienced, collaborative, and supportive group of pathologists, where career growth is actively encouraged.

Then Responsibilities as

Responsibilities

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  Qualifications

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  • ... each bullet. Pay as

    Pay

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    Compensation Overview New Brunswick - NJ - US: $238,970 - $289,574 The starting pay range(s) listed above is for full-time employees (FTE). You may also be eligible for additional discretionary incentive cash and stock opportunities. We determine starting pay thoughtfully – carefully considering the nature of the role, required skills, work location, schedule and the knowledge and experience you bring. Final compensation is guided by pay equity principles and applicable employment laws. Compensation programs are reviewed on an ongoing basis and may be adjusted over time to reflect evolving market factors, and individual, team or Company performance.

    Benefits as

    Benefits

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    ... the benefits paragraph. We should not include How We Work etc. We must ensure we preserve all substantive information from those sections. Let's extract the exact text. Position Summary text: "BMS is seeking a veterinary Clinical Pathologist to join a large and well-established biopharmaceutical company dedicated to developing safe and efficacious medicines for areas of unmet need. This is an exciting opportunity to work within a highly experienced, collaborative, and supportive group of pathologists, where career growth is actively encouraged." We also have earlier paragraph about culture etc. That is substantive; we should keep. Key Responsibilities list: - Provides expert scientific interpretation and integration of clinical pathology data from nonclinical development studies. - Scientific advisor to the Clinical Pathology laboratory in New Brunswick and collaborates with other functions within Nonclinical Drug Development Sciences (NDDS). - Reviews non-GLP and GLP study protocols and provides input into the design of clinical pathology endpoints and analyses. - Prepares clear, accurate, and scientifically rigorous clinical pathology reports that communicate the significance of findings for nonclinical safety assessment and regulatory submissions. - Serves as an independent clinical pathology scientific reviewer for outsourced toxicology studies. - Provides expert consultation on unusual or complex clinical pathology findings, including cytology, bone marrow aspirates, urine sediment, and exploratory biomarker selection, and participates in multifunctional investigative toxicology teams, as needed. - Collaborates with NDDS colleagues to optimize use of clinical pathology resources across various BMS sites (as feasible). - Continuously evaluates and applies new scientific methodologies to meet research and drug-registration needs and resolve toxicity-based issues. - Fosters an environment of scientific excellence, open communication, and creativity to maximize productivity and support employee career development. - Encouraged to present at scientific meetings and publish in peer-reviewed scientific journals. Qualifications list: - Advanced degree (DVM, and preferably MS or PhD or equivalent), and ACVP board certification in Clinical Pathology or “board eligible” with a solid foundation in Industry clinical pathology, toxicology, and related disciplines such as metabolism and pharmacokinetics. - Minimum of 8 years of relevant experience in the biopharmaceutical industry and/or a contract research organization (CRO), with substantial responsibility for interpreting clinical pathology data from nonclinical studies. - Demonstrated broad experience contributing to product registration activities, regulatory submissions, and supporting dossiers. - Solid understanding of GLP regulations and their application in an Industry clinical pathology laboratory environment. - Strong comparative clinical pathology expertise, including interpretation of data from toxicity and/or efficacy studies conducted in a diverse array of nonclinical species. - Comprehensive knowledge of the drug discovery and development process, including the biology and pathophysiology of one or more disease target areas. - Exceptional written and oral communication skills, with the ability to produce clear, accurate, and concise regulatory reports. - Strong scientific problem-solving skills with the ability to interpret and integrate diverse data types. - Experience serving on or leading cross-functional teams, with strong interpersonal skills and the ability to align people, resources, and activities with departmental and divisional objectives. - Demonstrates scientific leadership with the capacity to drive issue resolution and influence the direction of discovery or development programs. - Potential and ambition to take on an expanded leadership role within the Pathology department or cross-functional project teams in the future. - We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway. Compensation Overview text: "New Brunswick - NJ - US: $238,970 - $289,574 The starting pay range(s) listed above is for full-time employees (FTE). You may also be eligible for additional discretionary incentive cash and stock opportunities. We determine starting pay thoughtfully – carefully considering the nature of the role, required skills, work location, schedule and the knowledge and experience you bring. Final compensation is guided by pay equity principles and applicable employment laws. Compensation programs are reviewed on an ongoing basis and may be adjusted over time to reflect evolving market factors, and individual, team or Company performance." Benefits text: "Subject to the terms and conditions of the applicable plans then in effect, you may be eligible to participate in our comprehensive benefit plans – including wellbeing support, retirement and financial protection benefits, and insurance offerings (medical, dental, vision, life and disability). U.S.-based exempt employees are eligible for Flexible Time Off (FTO), which provides paid time off without a set accrual limit, subject to manager approval, along with 11 paid company holidays each year. Non-exempt employees, RayzeBio employees, and employees located in Puerto Rico receive 160 hours of paid vacation annually for new hires (subject to manager approval), 11 paid company holidays, and 3 optional holidays. Depending on eligibility, employees may also have access to additional time-off benefits, including paid sick leave, up to two paid volunteer days per year, summer hours flexibility, and leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs. Eligible employees also enjoy an annual Global Shutdown between Christmas Day and New Year's Day. U.S.-based job seekers can explore full benefit offerings at https://careers.bms.com/benefits" We need to ensure we don't include any boilerplate like "Subject to the terms and conditions..." is okay as it's substantive benefits. Now produce HTML. We must not include any extra text outside HTML. Let's craft:

    About the role

    At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it. BMS is seeking a veterinary Clinical Pathologist to join a large and well-established biopharmaceutical company dedicated to developing safe and efficacious medicines for areas of unmet need. This is an exciting opportunity to work within a highly experienced, collaborative, and supportive group of pathologists, where career growth is actively encouraged.

    Responsibilities

    • Provides expert scientific interpretation and integration of clinical pathology data from nonclinical development studies.
    • Scientific advisor to the Clinical Pathology laboratory in New Brunswick and collaborates with other functions within Nonclinical Drug Development Sciences (NDDS).
    • Reviews non-GLP and GLP study protocols and provides input into the design of clinical pathology endpoints and analyses.
    • Prepares clear, accurate, and scientifically rigorous clinical pathology reports that communicate the significance of findings for nonclinical safety assessment and regulatory submissions.
    • Serves as an independent clinical pathology scientific reviewer for outsourced toxic