• Contribute to the scientific roadmap for Protocol AI and ensure all outputs reflect current scientific and clinical best practices

• Develop and enhance scientific methodologies, structured authoring principles, and clinical trial design logic within the platform

• Monitor scientific, biomedical, and regulatory developments to keep Protocol AI scientifically robust and aligned with industry standards

• Collaborate with Product, Engineering, and AI teams to ensure scientific accuracy, clinical relevance, and high-quality feature development

• Serve as the primary scientific/medical escalation point for internal teams and external stakeholders

• Support onboarding, pilots, and enterprise implementations with strong scientific guidance

• Represent Risklick in conferences, panels, workshops, and scientific working groups

• contribute to scientific publications, white papers, case studies, and educational content promoting structured and digital-first protocol development

Required Qualifications

• Degree in scientific/life-sciences field. PharmD, or MD preferred

• Minimum 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

• Ability to work independently, multi-task, and work in a fast-paced environment

• Strong analytical and problem-solving ability; able to evaluate scientific inputs, identify gaps, and propose evidence-driven improvements

• Comfortable to use AI-enabled tools and technologies within scientific and clinical contexts

Bonus Skills

• Experience implementing study designs and clinical protocols using digital solutions

• Understanding of data models and clinical standards (CDISC, SNOMED, MeSH, MeDRA, ontologies)

What We Offer

• A potential strategic leadership role in a fast-growing Swiss company

• Opportunity to contribute to the future of an end-to-end digital study design and protocol development ecosystem.