26 switzerland English-speaking jobs in Opfikon

Leads end-to-end product strategy for a late-stage development asset, from research transition through commercialization and lifecycle management. Represents the asset at senior governance forums and leads a global, cross-functional Product Strategy Team. Owns the product strategy plan, drives it through governance, and ensures the organization makes timely decisions.

The Associate Director, Statistical Programming provides leadership and expertise in developing and maintaining statistical programming capabilities. This role works closely with the Director, Statistical Programming and Statisticians to ensure accurate and timely delivery of programming tasks for clinical trials and integrated analyses. The individual may manage Therapeutic Areas or programs, overseeing CRO delivery or in-house programming of data sets, outputs, and DDT files.

The Manager, Clinical Trial Authorization (CTA) ensures CTA activities for assigned clinical studies are planned, governed, and overseen in line with regulatory expectations and development timelines. The role translates global CTA direction into study-specific approaches, provides guidance to Study Teams and partners, and acts as the first line CTA point of contact. The Manager oversees outsourced CTA activities, ensures compliance with GCP requirements, and drives process improvements.

Senior Scientist responsible for designing, overseeing, and interpreting nonclinical PK/QSP studies to support regulatory submissions and drug development. Conducts PK, PBPK, QSP modeling and collaborates with internal stakeholders. Requires a Bachelor's, Master's, or Ph.D. in Life Sciences with 3+ years of pharmaceutical development experience.

Leads the design, execution, and interpretation of pharmacokinetic (PK) and toxicokinetic (TK) strategies for drug discovery, nonclinical, and development programs. Supervises and mentors a team of PK Scientists. Oversees the planning, execution, and interpretation of PK/TK studies. Collaborates with Research, NCD, and development functions.

Develops global regulatory strategies for assigned products, ensuring innovative and scientifically sound approaches from early development through post-marketing activities. Leads Global Regulatory Affairs Strategy Team and collaborates with Product Strategy Teams, Clinical Development Teams, and other stakeholders.