Clinical Scientist, Oncology (Non MD) Early Clinical Development
EU BASED ROLE About the Role The Clinical Scientist, Oncology at Pi Health will play a crucial role in leading the medical and clinical aspects of our innovative healthcare technology solutions. You will lead the design, conduct, analysis, and reporting of clinical trials, applying scientific training and clinical research experience to support all aspects of drug development — from facilitating the transition of molecules from pre-clinical discovery through the achievement of clinical proof of concept to supporting the registration and commercialization of a product. You will participate in cross-functional teams to generate, deliver, interpret and communicate high-quality clinical data supporting overall product scientific and business strategy. What You'll Do • Be accountable for the clinical aspects of design and conduct of one or more oncology clinical trials with a focus on early phase (Phase I–II), in collaboration with the medical monitor, clinical operations lead, and other colleagues • Lead the development of clinical protocols, protocol amendments, investigator brochures, Annual Reports, IND sections, CSRs, and other regulatory documents, publications, abstracts, and presentations • Together with Clinical Operations, be responsible for timely execution of all FIH programs through proof-of-concept, delivering innovative clinical study designs and high-quality trial execution • In collaboration with the medical monitor and biostatistician, conduct data review, analysis and interpretation of clinical trial data, regular review of individual subject safety data, and review of cumulative safety data • Establish and support relationships with external experts, consultants, key opinion leaders, regulators, and disease-specific investigator networks • Ensure implementation of latest clinical thinking and guidelines into clinical development plans and study designs Qualifications • Advanced life science degree (e.g. PhD, PharmD, RN) • At least 2 years in a clinical scientist role in the pharmaceutical industry executing oncology clinical trials • Demonstrated experience in oncology drug development with cross-functional knowledge (clinical ops, biostatistics, regulatory, clinical pharmacology, pharmacovigilance, and safety reporting) • Proven scientific writing skills and strong communication skills • Strong interpersonal skills with ability to build consensus and drive change across all levels of the organization • Critical thinker who is proactive with a highly collaborative style and team-focused approach • Ability to perform complex data analysis Nice to Have • Interest in AI, digital innovation, and digital health