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Senior Clinical Lead, Early Clinical & Experimental Therapeutics

Scorpion Therapeutics

Main Responsibilities Design safe, rapid, informative First-In-Human (FIH) oncology studies (incl. natural history, experimental model validation, mechanistic/signal-seeking, Proof-of-Mechanism/Proof-of-Concept) to support early Go/No-Go and pharmacokinetic decisions. Plan clinical development steps and integrate into overall development strategy; provide medical/clinical guidance for preclinical data generation/interpretation. Make front-line decisions on protocol design/execution, dose escalation, safety, and regulatory-facing information. Supervise clinical study execution; oversee and perform medical monitoring. Review/interpret results and author ECET-related documentation (consent forms, protocols, study reports; plus clinical pharmacology/ECET components of relevant documents). Coordinate oversight of CROs/outsourced activities; ensure cross‑functional communication; lead dose escalation meeting; review adverse event reports; oversee safety monitoring. Participate in data review/validation; prepare Key Results Memo and Clinical Study Report. Study Medical Manager (selected studies) Design and conduct FIH to phase 2a studies within timelines; review/approve study documents; coordinate setup/follow-up; ensure Ethics Committee/Health Authority documentation. Qualifications (Education/Experience) M.D. or M.D./Ph.D. 3+ years clinical research experience (Phase 1/2a patient oversight and interpreting preclinical/biomarker data). Experience designing/executing early development/exploratory studies; leading cross‑functional teams; medical safety oversight. Experience in translational/biomarker research and using emerging digital/AI tools. Skills/Requirements Biomedical knowledge; GCP knowledge; strong verbal/written communication; risk‑management mindset; matrix working; international/intercultural collaboration. Preferred MD+PhD (or equivalent bench experience); Global pharma experience; Combination therapy/cytoplasmic signaling targets; Late‑phase trial experience. Benefits (selected) Health and wellbeing benefits At least 14 weeks’ gender‑neutral parental leave #J-18808-Ljbffr Scorpion Therapeutics

Vacancy posted 1 day ago
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