Clinical Development Associate Medical Director- gMG

Role: Chief Medical Lead for clinical trials, serving as Medical Monitor and overseeing study strategy, design, execution, and safety monitoring. Responsibilities include developing key study documents, participating in cross-functional Study Execution Teams, providing scientific input for regulatory submissions, and liaising with internal groups and external medical personnel. Qualifications: MD, DO, or equivalent medical degree; typically 8+ years of experience in clinical or academic research; strong communication and collaboration skills; familiarity with GCP, biostatistics, pharmacology, and regulatory processes. Preferred: Board certification/eligibility, global clinical research experience, and clinical specialty training. HighValue: global clinical trials, medical monitoring, regulatory documentation, GCP, cross-functional coordination, and hybrid/worksite flexibility.