Senior Clinical Pathologist

WuXi AppTec Group; United States; On-site; USD 120,000 - 180,000; Full time

Job summary

WuXi AppTec Group is hiring a Senior Clinical Pathologist to lead interpretation of hematology, clinical chemistry, urinalysis, and cytology data for nonclinical studies. You will prepare clinical pathology sections in reports and collaborate with Study Directors to ensure rigorous quality and regulatory alignment.

The role requires a DVM/VMD or equivalent, ACVP certification, and 3+ years’ CRO experience. You will oversee bone marrow and blood smear evaluations, contribute to protocol

Qualifications

• Effective written and verbal communication skills.
• Ability to handle multiple projects, prioritize work, and meet deadlines.

Responsibilities

• Assist Study Directors in interpretation of clinical pathology data and preparation of clinical pathology sections in study reports.
• Serve as Study Clinical Pathologist or Principal Investigator; attend all key activities of preclinical studies regarding clinical pathology, evaluate data, and write a comprehensive clinical pathology report.
• Examine bone marrow smears, blood smears, urine, body fluids and other related preparations.
• Collaborate with Anatomic Study Pathologists to ensure relevant correlations and interpretation for clinical and anatomical pathology findings.
• Contribute to protocol development of research studies.
• Communicate with sponsors to answer questions and discuss results regarding the clinical pathology report.
• Provide expertise in method development and instrumentation; assist in expanding clinical pathology assays.
• Conduct planned, long-term internal education and training.
• Provide guidance to Clinical Pathology personnel with technical issues.
• Perform other related duties as assigned.

Skills

Communication

Prioritization

Multitasking

Education

DVM/VMD

PhD in Clinical Pathology

Job description

Overview

Contribute to all aspects of clinical pathology conducted on nonclinical studies. Collaborate with Study Directors and Study Pathologists to provide comprehensive interpretation of hematology, coagulation, clinical chemistry, and urinalysis data, evaluate cytology of bone marrow and blood smears, and prepare the clinical pathology portions of reports.

Responsibilities

• Assist Study Directors in the interpretation of clinical pathology data and preparation of clinical pathology sections in the study reports.
• Serve as Study Clinical Pathologist or Principal Investigator; attend all key activities of preclinical studies regarding clinical pathology, evaluate hematology, coagulation, clinical chemistry, and urinalysis data, and write a comprehensive clinical pathology report.
• Examine bone marrow smears, blood smears, urine, body fluid, and other fluid preparations related to the studies.
• Collaborate with Anatomic Study Pathologists to ensure relevant and appropriate correlations and interpretation for clinical and anatomical pathology findings.
• Contribute to protocol development of research studies.
• Communicate with sponsors to answer questions and discuss results regarding the clinical pathology report.
• Provide expertise in method development and identification and evaluation of new instrumentation. Assist in expanding the array of clinical pathology assays.
• Conduct planned, long-term internal education and training
• Provide expertise and guidance to Clinical Pathology personnel with technical issues.
• Perform other related duties as assigned.

Qualifications

• DVM/VMD (Doctor of Veterinary Medicine) degree or equivalent required. Ph.D. in Clinical Pathology or related discipline preferred.
• ACVP Board Certification in Clinical Pathology required.
• 3+ years of related experience in clinical pathology from contract research organizations.
• Effective written and verbal communication skills.
• Ability to handle multiple projects, prioritize work, and meet deadlines.

This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. Employees holding this position will be required to perform any other job-related duties as requested by Management.

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, or protected veteran status and will not be discriminated against on the basis of disability.