330486BR
Oct 22, 2021
USA

Job Description

The number 1 cause of death in men and women globally is cardiovascular diseases, taking an estimated 17.9 million lives each year (nearly a third of all death). Novartis is committed to developing transformative treatments for cardiovascular and metabolic diseases, including heart failure, arrhythmias and atherosclerotic cardiovascular disease, as well as diseases across a wide range of therapeutic areas.

The Novartis Institutes for BioMedical Research (NIBR) is the innovation engine of Novartis that collaborates across the company and beyond, focusing on powerful new technologies that have the potential to help produce therapeutic breakthroughs for patients. Translational Medicine (TM) is the clinical research arm of NIBR, and includes about 900 associates globally. TM plays a pivotal role in bringing innovative medicines to patients, by building on research advances to develop new therapies, and bridging drug discovery and clinical application.

The TM Discovery & Profiling (TMDP) is a group of physicians and clinical researchers who drive innovative science from discovery to the patient through the selection, profiling, and effective development of medicines. Translational medicine experts oversee Phase 1 and 2 clinical trials to demonstrate proof-of-concept (PoC) in patients, as well as support for Phase 3 development. Translational medicine experts are key and highly visible members of global cross-functional project teams that design and implement early research and discovery projects that then culminate in clinical PoC studies. Translational medicine experts collaborate with colleagues in biology and chemistry to identify targets in diseases with significant unmet medical needs and provide input on likely clinical development pathways. The PoC studies led by our translational medicine experts are among the most critical steps in drug development at Novartis. After PoC and if the program proceeds to full development, the translational medicine expert continues as a key member of the full development team up to and including registration.

As a Cardiovascular Metabolism (CVM) Profiling TM Expert, you will collaborate with the CVM TM Head or other experienced TM Expert to develop high value decision-strategies for the Translational Medicine component of drug development projects and lead global cross-functional project teams through the PoC phase and beyond. You will be responsible for implementation of strategies for assigned drug development projects in liaison with appropriate line functions and leading to clinical pharmacology and profiling studies that meet regulatory requirements (ICH/GCP, Novartis SOPs/NIPs).

Your main accountabilities will be:

• Lead global project teams through PoC phase to drive implementation of the PoC strategy; participate in project teams through program life cycle from NTRC to registration.
• Responsible for clinical portions of the Integrated Development Plan (IDP) through PoC.
• Responsible for implementation of studies during the PoC phase by providing medical and scientific leadership and expertise to all line functions on the project team. This may include methodology studies to identify and validate novel endpoints for early decision making in PoC studies.
• Act as medical monitor for one or more global clinical studies.
• Communicate clinical team matters to project teams and relevant Decision Boards (DADB).
• Convene relevant (internal and external) leaders together to consider the proposed approach to PoC.
• Evaluate clinical centers and foster communication with crucial collaborating investigators.
• Oversee publication and external presentation of PoC clinical study results.
• Accountable for compound related biomarker strategies; works closely with Biomarker Experts in implementation.
• In collaboration with research scientists, identify, develop, and implement strategy for preclinical support of program-related objectives. This includes assessment of medical need, proposal of clinical development pathways, and review of preclinical data for clinical implications, and other relevant activities.
• Participate in team presentations to health authorities as the TM expert.

Position can be based in Basel, Switzerland or Cambridge USA.

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

Minimum requirements

What you bring to the role:

- Doctoral degree, MD required with clinical subspecialty training preferred in cardiovascular and metabolic disease
- At least 5 years’ experience in a pharmaceutical/biotech company, CRO, or academic medical center, or related clinical research/trials experience
- Specialized training in clinical pharmacology or experience working in the field of clinical pharmacology
- Specialized training in the cardiovascular and metabolic disease therapeutic area or clinical research experience in this therapeutic area
- Documented Clinical Trials experience able to serve as internal TM expert for TA
- Significant contributions to a field over time, creates new concepts
- Strong publications record with nationally recognized reputation
- Demonstrated passion for discovery clinical trials and profiling science.

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.
Imagine what you could do at Novartis!

This is a dual level posting. This position is written for Director level. To be considered at the Executive Director you must have significant related Pharma career experience.
NIBR
Translational Medicine
USA
Cambridge, MA
Switzerland
Research & Development
Full Time
Regular
No
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330486BR

Cardiovascular Translational Medicine Expert (Director/Exec Director)

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