N

NAMSA

MedTech CRO delivering end-to-end device development

Associate Director - Regional Pathology

Biology & BiotechConfirmed live in the last 24 hours
Full-timeRemote in USA$152.3k - $296.6k /yrRemote

About the Job

Requirements

  • A Doctor of Veterinary Medicine (DVM) or Medical Doctor (MD) degree from an accredited university is required.
  • Three years of related work experience is required.
  • The employee must maintain board certification requirements.
  • The role requires regular exposure to livestock, domestic animals, and laboratory animals, and to sharp objects, formaldehyde, and other toxic or caustic chemicals; occasional exposure to fluoroscopy, blood-borne pathogens, and zoonotic diseases may occur.
  • The role requires standing, handling objects and tools, reaching, talking, hearing, and computer work; frequent walking and sitting; occasional use of cutting tools; and occasional lifting or moving up to 50 pounds, or up to 100 pounds with assistance.
  • Specific vision abilities required include close, distance, and color vision, depth perception, and the ability to adjust focus.

Responsibilities

  • Provide scientific oversight and guidance for regional anatomic pathology evaluations; review study protocols, proposals, and study designs; and support clients and regulatory agencies with study interpretation, regulatory submissions, and scientific consultations.
  • Ensure pathology assessments meet applicable Good Laboratory Practice (GLP), OECD, FDA, ISO, and other regulatory or compendial requirements, and maintain consistent, high-quality, accurate diagnoses across pathologists and sites.
  • Serve as a pathology subject matter expert and perform evaluations and slide reviews as needed to meet study timelines, client commitments, and business needs.
  • Lead regional pathology operations, optimize workflows, monitor departmental metrics and operational dashboards, and collaborate with histology, necropsy, study direction, quality assurance, and laboratory operations teams on continuous improvement.
  • Support the introduction, validation, and implementation of pathology methodologies, technologies, and services; plan staffing and resources to meet business demands.
  • Directly manage and develop US-based pathologists and pathology staff, including performance management, coaching, performance reviews, succession planning, career development, recruitment, hiring, onboarding, retention, workload assignment, and resource allocation.
  • Develop pathology training and competency-assessment programs; coordinate peer review and diagnostic quality initiatives; maintain competency evaluation and quality oversight programs.
  • Ensure compliance with GLP regulations, client requirements, standard operating procedures, and applicable regulatory standards; support internal audits, regulatory inspections, client audits, and corrective actions.
  • Partner with senior leadership on departmental goals, growth strategies, and operational plans; identify service-expansion opportunities; and contribute to revenue growth through operational efficiencies, expanded capacity, and scientific consultation.
  • Participate in business development, client interactions, and proposal development; represent the organization at conferences, industry meetings, professional societies, and compendial working groups.
  • Serve as study pathologist for nonclinical studies compliant with FDA and other regulatory standards; develop protocol pathology methodologies; interpret gross, microscopic, and clinical pathology data as applicable; consult with clients and study directors; and complete timely, accurate study reports.
  • Collaborate with facility veterinarians to generate diagnostic pathology data and interpret results in support of colony health; participate in necropsies as appropriate and train associates participating in necropsies.
  • Provide technical guidance to histologists on histological preparations and train department personnel in gross pathology and histology procedures in line with client goals, organizational needs, and company policy.
  • Complete study reports and pathology assignments according to management prioritization schedules; work with Quality and Scientific Affairs to maintain study integrity and GLP-compliant processes.
  • Represent the organization through seminars, client visits, and shows, including writing articles for publication or presentation.
  • Maintain a GLP-compliant workspace, perform required calibration and validation activities, operate equipment, and perform work in compliance with applicable standard operating procedures.
  • Assist in research to develop techniques for identifying and interpreting pathological conditions.
  • Perform pathology evaluations, microscopic examinations, peer reviews, and consultations as needed to meet client commitments, support business demands, expand department capacity, and maintain diagnostic competency and board-certification requirements.
  • Perform other duties as assigned.

Desired Qualifications

  • Board certification in anatomic pathology by the American College of Veterinary Pathologists (ACVP), the European College of Veterinary Pathologists (ECVP), or an equivalent body is desired.

About the Company

NAMSA

MedTech CRO delivering end-to-end device development

NAMSA is a medical device-focused contract research organization (CRO) that provides end-to-end development services. It helps sponsors bring medical devices to market by offering testing, regulatory and quality consulting, reimbursement support, and clinical research. The way it works is through a global team with regulatory expertise and therapeutic knowledge who guide and perform the work needed across the product development lifecycle, from initial testing to regulatory clearance, reimbursement, and commercialization. NAMSA differentiates itself with its worldwide regulatory know-how, depth of therapy-specific expertise, and a commitment to delivering proven, cost-effective solutions that speed up development. The company’s goal is to accelerate medical device product development and successful commercialization by providing comprehensive, reliable services and guidance from concept to market.

Company size
1,001-5,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Toledo, OH
Founded
1967

Recently Posted Jobs

Explore more opportunities at NAMSA

See more jobs