10 switzerland English-speaking jobs in Allschwil

: 3 years Percentage: 100%, primarily on-site with flexibility for home office Location: Allschwil, Switzerland

As a Field Engineer, you will perform maintenance, qualification, and calibration of SKAN systems in the pharmaceutical sector. You will travel throughout Europe, troubleshooting and repairing isolators, and documenting test reports.

Leads global access strategies by designing and driving health economic and evidentiary approaches for HTA and payer submissions. Designs and delivers robust evidence packages to support HTA bodies and payer decisions.

Information Security Specialist needed to support colleagues and protect IT assets. Partner with infrastructure teams on audits, conduct internal audits, and monitor security controls. Manage vulnerabilities, advise on security risks, and support customer inquiries. Requires a Master's degree in computer science, industry recognized security qualifications, and 5+ years of experience.

Leads the design and conduct of observational research to support drug development strategies, regulatory approvals, and payer/HTA/provider engagements. Serves as statistical lead and subject matter expert for RWE/HEOR research design, methodologies, and data analysis. Develops study protocols, statistical analysis plans, and study reports. Collaborates with internal and external stakeholders to ensure project timelines and goals are met.

Develops clinical pharmacology strategies for assigned therapeutic areas, oversees pharmacokinetic and pharmacodynamic activities, and contributes to clinical protocol development. Provides expertise to cross-functional project teams, supports regulatory submissions, and represents Neurocrine at meetings with global health authorities.

Information Security Specialist needed to ensure ISO/IEC 27001, SOC1, and SOC2 compliance. Conducts internal audits, manages vulnerabilities, and provides security risk advice. Requires a master's degree, industry security certifications (CISSP preferred), and 5+ years of relevant experience.

Provides strategic regulatory leadership for programs, overseeing all regulatory activities across the product lifecycle. Drives collaboration with cross-functional partners to ensure consideration of regulatory perspectives. Serves as a trusted advisor across the company and may be recognized as an expert externally.

Directs Phase 1-3 clinical trials, develops study protocols, and collaborates with multidisciplinary teams. Responsible for clinical trial program oversight, resource planning, and communication with internal and external stakeholders. Requires MS degree in Life Sciences or related field with 10+ years of experience in industry or equivalent combination of education and experience. Expertise in drug development, operations, and strategic planning is essential.

Technical Writer needed to ensure accuracy of product information and maintain AMOS documentation. Collaborate with development and product teams to understand features and workflows. Strong writing, editorial, and communication skills required. Native-level English or equivalent communication skills.