Associate Director, Anatomic Pathology

Aug 03, 2021

Job Description

5600! 5600 scientists working on 340 discovery programs in 8 disease areas focusing on 90 new molecular entities makes Novartis the premier place to develop your career as a pharmaceutical professional. If you are curious, scientifically minded, and want to positively impact society by speeding delivery of novel therapies to needy patients, then look no further, NIBR is the place to be.

In the role of anatomic pathologist within NIBR's Translational Medicine team you will provide expertise to research and preclinical safety studies through well-written reports that accurately reflect data derived from standard and innovative anatomic pathology endpoints as well as investigative biomarkers and molecular assessments. In conjunction with the study teams, you will contribute an integrated assessment of the significance of study findings to human safety within regulatory submission packages. You will also actively participate in the global drug development process through contributions as a Project Pathologist on assigned drug targets and also has the opportunity to serve as the safety assessment expert on project teams. In addition, you will work collaboratively within our pathology and investigative safety teams to build our scientific and technical expertise in translational biomarkers and technologies used to support safety studies and in-vivo safety models.

Your major accountabilities will include but not be limited to:

• Effectively assess for pharmacological and toxicological effects of small molecules and biologics in preclinical studies, with a focus on anatomic pathology and pathology peer review.
• Collaborate with global team of pathologists and other scientists in design of preclinical safety studies and interpretation and communication of study findings, including the impact of the data on the safety profile and clinical development.
• Provide oversight and/or pathology peer review of protocols, data, and reports generated at contract laboratories and maintain effective relationships with CRO pathologists, scientists, and technical staff to ensure high quality, on-time reporting.
• Drive scientific and technical support for identification, development, qualification, and validation of translational biomarkers and pathology endpoints through collaboration with internal and external expert working groups.
• Serve as Project Pathologist on assigned compounds, targets, and therapeutic areas.
• Opportunity to participate as safety assessment expert on global drug development project teams

Diversity & Inclusion / EEO

The Novartis Group of Companies are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential.

Minimum Requirements

What you will bring to the role:

Minimum requirements :
• Doctor of Veterinary Medicine or equivalent
• Board Certification in Anatomic Pathology by European/American College of Veterinary Pathologists (ECVP or ACVP)
• Preferred: PhD in a biological science
• Experience in toxicological pathology. Preferred: Experience in biologics, gene and cell therapy and emerging/novel modalities application in safety assessment, preferably within pharmaceutical/biotech or contract research organization
• Good understanding of the drug development process, preferably including experience working directly on drug development project teams and Regulatory interactions and submissions
• Excellent verbal and written communication skills
• Ability to work cross-functionally within a team and matrix environment
• Experience with GLP regulations and peer review
• Experience with digital pathology systems

• Why consider Novartis?

769 million. That’s how many lives our products touched in 2020. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives?

We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges.

We are Novartis. Join us and help us reimagine medicine.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Commitment to Diversity & Inclusion:

Novartis is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve.
Translational Medicine
East Hanover, NJ
Research & Development
Full Time
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Associate Director, Anatomic Pathology

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