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Senior Translational Pathologist

2 months ago


New Providence, Iowa, United States 1925 GlaxoSmithKline LLC Full time
Unlock Your Potential in Precision Medicine

As a translational and computational pathologist, you will be part of a dynamic team driving innovation in precision medicine at GSK. Our organization is dedicated to bringing new medicines to patients in need, and we're seeking a skilled professional to join our ranks.

Key Responsibilities:
  • Develop and refine clinical development strategies for oncology, respiratory, immunology, and infectious diseases.
  • Collaborate with biomarker scientists, companion diagnostic scientific leads, and research unit experts to enable rigorous biomarker and diagnostics plans.
  • Lead clinical biomarkers assay and companion diagnostics development, oversight, and strategy, both internally and externally with CROs and partners.
  • Build high-innovation clinical-grade bioassays to fulfill study program needs.
  • Drive collaboration with our AI/ML organization to develop state-of-the-art computer vision digital pathology quantitative tools.
  • Review protocols, amendments, and revisions, and participate in study governance to ensure efficient and successful study execution.
  • Support companion diagnostics across the business, interface with regulatory authorities, and prepare submission documentation.
  • Participate in clinical trials advisory boards, seek input from key opinion leaders, and deliver concise recommendations to study teams.
  • Interface with external KOLs, clinical trial sites, technology vendors, and business development partners.
Requirements:
  • MD or DO degree from an accredited training program and board certification (or local equivalent).
  • Residency Anatomic Pathology (AP) or combined Anatomic Pathology/Clinical Pathology (AP/CP) training and American Board of Pathology (ABP) board certification (or equivalent).
  • Surgical Pathology subspecialty training and board certification.
  • Skills in laboratory medicine, including molecular genetic pathology, flow cytometry, assay development, and validation.
  • Experience in pathophysiology of human diseases and clinical practice.
  • 5+ years of relevant clinical work experience, including medical education in hospital, outpatient clinic, and other medical environments.
  • 2+ years of additional postgraduate clinical work experience.
  • Experience in diagnostic pathology and laboratory medicine, including image analysis tools and whole slide image review.
  • Data and science experience, including basic statistics, quality assurance, and experimental controls.
Preferred Qualifications:
  • Master's level degree (MS, MEng, MPH) and/or Ph.D. in a related field with bench wet-lab experience.
  • Pharmaceutical industry experience in translational biomarkers, clinical development, field, or discovery.
  • Ability to interface with quality teams across the organization.
  • Immunohistochemistry, molecular/genomics/NGS, and flow cytometry assay validation, review, creation, optimization, and data reporting.
  • Track record of regulatory engagements.
  • Clinical trials matrix team experience.
  • Track record of companion diagnostics development in IHC, molecular genetic pathology, flow, or other areas.
  • Additional board certification in other pathology subspecialties.
  • Experience in digital pathology, image analysis, data science, computer programming, and related investigative methods.
  • Experience in clinical and research laboratory setup, leadership, public speaking, education of histo-technologists, trainees, allied health professionals, inspection, and quality monitoring in anatomic pathology.
  • Clinical trials support, protocol and study documentation review/authorship, contract research organization interfacing, multinational matrix influencing skills.

We offer a comprehensive benefits program and a dynamic work environment that fosters innovation and collaboration. If you're passionate about precision medicine and want to make a meaningful impact, we encourage you to apply.