Clinical Scientist

Role: Clinical Scientist specializing in oncology and radiopharmaceuticals, responsible for protocol development, scientific document drafting, and driving medical monitoring in clinical studies. Responsibilities include designing studies, collaborating with key opinion leaders, supporting regulatory submissions (INDs, CTAs), overseeing data review, safety assessments, and ensuring compliance with GCP and ICH guidelines. The role involves developing training for clinical sites, contributing to study reports, and optimizing study designs for early-phase radiopharmaceutical therapies. Qualifications: Advanced degree (PhD, MD, PharmD, etc.) preferred; 3+ years of clinical research experience, particularly in oncology, nuclear medicine, or radiopharmaceuticals; hands-on experience with protocol development, regulatory submissions, and clinical data review; strong medical writing and communication skills. High-Value: Oncology, radiopharmaceuticals, targeted radiotherapy, early-phase clinical development, regulatory interactions with FDA/EMA, GCP compliance, clinical trial design, and cross-functional collaboration. Travel requirement up to 20%, with domestic and international travel possible.