Senior Clinical Scientist

Role: Senior Clinical Scientist supporting phase 1-3 clinical development programs for endocrine-related therapies at Crinetics. Responsibilities: monitor, analyze, and review clinical trial data; collaborate with cross-functional teams (Medical Lead, Clinical Operations, Biometrics, Pharmacovigilance, Medical Affairs); author/review protocols, safety narratives, and regulatory documents; support safety reviews and data integrity; engage with investigators, CROs, and key stakeholders. Requirements: MD, Ph.D., Pharm.D., or equivalent with 8-10 years industry experience, including 3-5 years in clinical research within biopharma; strong knowledge of FDA/EMA regulations, GCP, ICH guidelines; proficiency in clinical data review, safety monitoring, and medical monitoring activities; excellent collaboration and communication skills. Preferred: experience in endocrine disorders or related therapeutic areas, laboratory environment familiarity, and regulatory submission support. High-value: expertise in clinical trial monitoring, safety data analysis, protocol development, and cross-functional collaboration within early to late-phase clinical trials. Work setup: primarily office-based with up to 5% travel.