Prepares photographic or video images of pathology specimens for use in group or project presentations, reports, publications and/or presentations
Anatomic pathology evaluation of investigative pathology and regulatory toxicity studies from lead identification/optimization through registration and post-marketing approval
Participation in regulatory submission document preparation, poster presentations and scientific publications, including addressing queries from global health authorities
The position includes opportunities for potential additional roles including:
Preclinical safety representative on discovery and/or development project teams
Minimal Requirements :
DVM or equivalent and ACVP/ECVP board certification in veterinary anatomic pathology
PhD in a relevant scientific discipline is strongly preferred
1-3 years of experience in discovery and/or toxicologic pathology in the pharmaceutical/biotechnology sector, or in the gross and histologic assessment of laboratory animals
Practical experience using imaging technologies and molecular diagnostic pathology techniques to understand the pathologic basis of disease and support drug discovery and development would be preferred
Demonstrated excellence in oral and written communications, strong interpersonal skills, critical thinking and issue resolution skills, and scientific collaboration, guidance, and mentoring of non-DVM scientists and laboratory associates
Ability to contribute to decision making in a manner that is timely and consensus based, and to foster productive dialogue on complex topics
Experience with new modalities (genetic and cell therapies) as well as experience in IHC/ISH, multiplex imaging, digital pathology tools, and interpretation of tissue-based biomarkers would be a plus
Drive the adoption of innovative AI-powered solutions to enhance efficiency and accuracy in histopathology processes
#LI-KM4
Pay Range:
$180,000 - $270,000
Disclosure Statement:
Flex Designation:
On-Site Designated
Flex Eligibility Status:
In this On-Site designated role, you will work five days per week on-site with ad hoc flexibility.
Note: The Flex status for this position is subject to Vertex's Policy on Flex @ Vertex Program and may be changed at any time.
#LI-Onsite
Company Information
Vertex is a global biotechnology compan
Benefits
Health insuranceDental insuranceVision insurance401(k)Equity / stock optionsPerformance bonus
Additional Information
Job Description
Pathology Senior Principal Research Scientist, Vertex Pharmaceuticals (Boston)
Preclinical Safety Assessment (PSA) is a global function responsible for the design and conduct of comprehensive nonclinical safety programs for the evaluation of Vertex therapies at all stages of discovery and development. Vertex Pharmaceuticals uses cutting edge science and technology to perform robust assessments of novel therapies for the treatment of the most serious diseases with unmet medical need. Our culture enables individual empowerment where We Wins , Fearless Pursuit of Excellence , and Innovation are more than just corporate values; they are part of our everyday lives. PSA pathologists have significant roles in the drug development process beginning in early discovery and continuing through the entire drug development value chain resulting in successful registration and marketing approval.
Vertex Pharmaceuticals · Boston, MA