Bringing life changing medicines to millions of people, Novartis sits at the intersection of cutting edge medical science and innovative digital technology. As a global company, the resources and opportunities for growth and development are plentiful including global and local cross functional careers, a diverse learning suite of thousands of programs & an in house market

Global RSC Director will be accountable for contributing to developing overall, cross functional programs of a priority disease area, especially early in lifecycle focused on shaping assets with strong commercial potential in line with TA priorities. The role provides direction and functional expertise in a cross functional RSC team and prioritizes US first with enhanced

1. Accountable for the operational delivery of the clinical development program and is responsible for the overall operational execution of the clinical program and related trials, as aligned with the IDP/CDP. 2. Single GCO point of contact for assigned clinical development program and related trials. 3. Key partner to GPCH during strategy, planning and execution stage of

$500 million! That's the savings Sandoz has provided in just two years to the US healthcare system as a result of the successful adoption of one of our oncology supportive care biosimilar into clinical practice. Sandoz has eight biosimilar approved globally including four in the US and more than ten in the pipeline. Biosimilar may enable more patients to access advanced b

Bringing life changing medicines to millions of people, Novartis sits at the intersection of cutting edge medical science and innovative digital technology. As a global company, the resources and opportunities for growth and development are plentiful including global and local cross functional careers, a diverse learning suite of thousands of programs & an in house market

$500 million! That's the savings Sandoz has provided in just two years to the US healthcare system as a result of the successful adoption of one of our oncology supportive care biosimilar into clinical practice. Sandoz has eight biosimilar approved globally including four in the US and more than ten in the pipeline. Biosimilar may enable more patients to access advanced b

100,000+ That's how many patients participate in our clinical trials at any given time. GCO is Novartis' powerhouse of Global Clinical Operations, redesigned to enable faster trial recruitment and enhanced trial delivery resulting in more timely access for patients to potential novel treatments. Every day, we are the link between science and medicine imagine the impact yo

40! The number of Clinical Submission Documents you will review as the new Sr QC Specialist based at Novartis in East Hanover, NJ. As part of Submission Management and Quality team, you will be responsible for conducting the clinical content review and identifying inaccuracies for preclinical and/or clinical documents (e.g. Summary of Clinical Efficacy, Summary of Clinica

Bringing life changing medicines to millions of people, Novartis sits at the intersection of cutting edge medical science and innovative digital technology. As a global company, the resources and opportunities for growth and development are plentiful including global and local cross functional careers, a diverse learning suite of thousands of programs & an in house market

If you are interested in the dynamic field of safety pharmacology, we have a role that encompasses nearly all aspects of the discipline. Partnering with external providers, oversight and monitoring of all ICH S7a guidance studies is a primary responsibility of the role. As well, connectivity with aspects of toxicology investigations (ECG subject matter expertise). Follow

Novartis Institutes for BioMedical (NIBR) is the global pharmaceutical research organization of Novartis. With approximately 6,000 scientists and physicians around the world, our research is focused on discovering innovative new drugs that will change the practice of medicine. We have an open and entrepreneurial culture, encouraging collaboration to make effective therapi

of the Role As the Director of the Clinical Product Line in SDP, you will lead, develop, and mentor a group of experienced product managers. Together with the team and key stakeholders, you will create and refine a sustainable vision for a group of globally deployed, high impact scientific software products crucial for NIBR clinical operations, and you will lead the team t

Scout for, evaluate, and execute high value drug product in licensing deals and portfolio expansion deals for Region International markets aligned to Regional and Global Business Development strategy. Manage assigned alliance relationships. Accountabilities Your responsibilities include, but are not limited to Support development of Regional Business Development strategy

$500 million! That's the savings Sandoz has provided in just two years to the US healthcare system as a result of the successful adoption of one of our oncology supportive care biosimilar into clinical practice. Sandoz has eight biosimilar approved globally including four in the US and more than ten in the pipeline. Biosimilar may enable more patients to access advanced b

The MSL is a field based, non promotional medical and scientific role. Their key objective is to demonstrate deep therapeutic expertise, understand territory/market influences, engage scientifically with HCPs and medical experts, manage and develop their territory and execute all relevant activities in alignment with the IDMT strategic and tactical plan while functioning