Senior Principal Scientist/in-vivo Pharmacology Lab Head (80-100%*) at Novartis

Basel, Basel-City, Switzerland -

Full Time

Start Date

Immediate

Expiry Date

14 May, 26

Salary

0.0

Posted On

13 Feb, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

In Vivo Pharmacology, Drug Discovery, Preclinical Research, Target Validation, Team Leadership, Rodent Experiments, PK/PD, Efficacy Studies, Target Engagement Biomarkers, Due Diligence, Matrixed Environment, Mentoring, Scientific Rigor, Renal Diseases, Liver Fibrosis, Ex Vivo Assays

Industry

Pharmaceutical Manufacturing

Description

Band Level 5 Job Description Summary Location: Basel, Switzerland Full time, #LI-Onsite Disease Area X, part of the Biomedical Research (BR) group at Novartis, is dedicated to advancing research on critical human organs, including the kidney, lung, and liver. We are seeking an experienced in vivo pharmacologist to join our interdisciplinary pharmacology team and help drive the development of novel medicines toward clinical application. In this role, you will be responsible for designing, executing, and implementing preclinical in vivo pharmacology strategies for drug discovery programs. You will lead a team of scientists in the conception, execution, and interpretation of in vivo and ex vivo studies that support new model development, target validation, and the progression of drug discovery projects. Additionally, you will collaborate closely with key matrixed functions within DAx and BR to ensure seamless advancement of drug discovery efforts and effective translation of scientific insights into clinical impact. Job Description Your responsibilities include, but are not limited to: Serve as the in vivo pharmacology lead on drug discovery project teams and act as lab head, overseeing a team of laboratory research scientists. Define and drive the in vivo pharmacology strategy for drug discovery projects, guiding multi-disciplinary project teams toward key decision milestones. Lead the design, execution, and interpretation of in vivo and ex vivo rodent experiments to support a portfolio of drug discovery programs, including new target identification, validation, and discovery of in vivo target engagement biomarkers Guide and mentor research scientists within the pharmacology discipline, fostering their development and scientific growth. Contribute to due diligence activities, manage external research collaborations, and oversee outsourcing of in vivo studies. Communicate and report project and team strategies, scientific vision, and data to key stakeholders in a clear and compelling manner. Essential Requirements - what you will bring to the role: Ph.D. or MD/Ph.D. in pharmacology, biology, or a related field, with ideally at least 3 years of postdoctoral experience. Minimum of 3 years’ experience in drug discovery, specifically in vivo preclinical research within the pharmaceutical or biotechnology sector. At least 3 years of proven expertise in leading high-performing in vivo pharmacology teams. Certifications required for conducting and supervising animal experiments (minimum LTK 2, or an equivalent FELASA Cat. C accredited course). Demonstrated expertise in leading preclinical animal model studies, including the design and execution of fit-for-purpose drug discovery in vivo flow charts (PK/PD, efficacy), and enabling deep mechanistic and pharmacological characterization of lead candidates. Strong preference for expertise in animal models of renal diseases and/or liver fibrosis/cirrhosis. Prior experience with ex-vivo rodent tissue molecular or biochemical assays is also preferred. Ability to effectively influence within a matrixed environment. Must be team-oriented, collaborative, and committed to mentoring and developing talent, while fostering a culture of curiosity, accountability, and scientific rigor. Excellent oral and written communication skills in English; proficiency in German is desirable. *Restrictions on flexible working arrangements may apply and will be discussed at interview if applicable Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to inclusion.switzerland@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Skills Desired Improving the lives of people living with disease takes more than innovative science. It takes a focus on the needs of people and a community committed to meeting them. It takes a team of people like you. Working together. Learning together. Thriving together. Discover how you can join us in changing people’s lives. In the context of China Cross-Border Data Transfer (CBDT) policy, if you need to apply for a position in China, please go to the local Recruiting System TaleNov .

Responsibilities

The role involves leading an in vivo pharmacology team responsible for designing, executing, and interpreting preclinical in vivo and ex vivo studies to drive drug discovery programs for critical human organs. Responsibilities include defining the overall in vivo pharmacology strategy and guiding multidisciplinary project teams toward key decision milestones.