ph3Senior Clinical Research Scientist (m/w/d) - 100% /h3pLocation: Bern /ppPosted: 12/1/2025 /ppWe are now seeking a passionate and highly skilled Senior Clinical Scientist to join our team. /ppbAbout Risklick /b /pprisklickpOur flagship product, Protocol AI, leverages artificial intelligence to empower clinical experts to design evidence-based clinical trial protocols, optimize study design, and generate high-quality protocols in a fraction of the time. We are transforming how clinical trial protocols are designed, written, and managed—enabling biopharma companies to develop truly digital, data-driven protocols for the future. /ppWe are now seeking a passionate and highly skilled Senior Clinical Scientist to join our team. In this role, you will play a key part in shaping and enhancing our AI-powered Protocol AI platform, helping us redefine protocol development and advance the next generation of clinical trial design. /ppbKey Responsibilities /b /pulliContribute to the scientific roadmap for Protocol AI and ensure all outputs reflect current scientific and clinical best practices /liliDevelop and enhance scientific methodologies, structured authoring principles, and clinical trial design logic within the platform /liliMonitor scientific, biomedical, and regulatory developments to keep Protocol AI scientifically robust and aligned with industry standards /liliCollaborate with Product, Engineering, and AI teams to ensure scientific accuracy, clinical relevance, and high-quality feature development /liliServe as the primary scientific/medical escalation point for internal teams and external stakeholders /liliSupport onboarding, pilots, and enterprise implementations with strong scientific guidance /liliRepresent Risklick in conferences, panels, workshops, and scientific working groups /lilicontribute to scientific publications, white papers, case studies, and educational content promoting structured and digital-first protocol development /li /ulpbRequired Qualifications /b /pulliDegree in scientific/life-sciences field. PharmD, or MD preferred /liliMinimum of 6 years of experience in clinical development with at least 4 years of clinical trial design and protocol development within pharma, biotech, or CRO organizations /liliAbility to work independently, multi-task, and work in a fast-paced environment /liliStrong analytical and problem-solving ability; able to evaluate scientific inputs, identify gaps, and propose evidence-driven improvements /liliComfortable to use AI-enabled tools and technologies within scientific and clinical contexts /li /ulpbBonus Skills /b /pulliExperience implementing study designs and clinical protocols using digital solutions /liliUnderstanding of data models and clinical standards (CDISC, SNOMED, MeSH, MeDRA, ontologies) /li /ulpbWhat We Offer /b /pulliA potential strategic leadership role in a fast-growing Swiss company /liliOpportunity to contribute to the future of an end-to-end digital study design and protocol development ecosystem. /li /ul /prisklick /p #J-18808-Ljbffr /p
Senior Clinical Research Scientist (m/w/d) - 100%
