Associate Scientific Director, Clinical Genetics

Role: Associate Scientific Director, Clinical Genetics, supporting late-stage clinical development through human genetics and pharmacogenomics expertise. Responsibilities: lead genetics strategies across Phase I-III trials, advise on protocol design, develop and oversee genetic testing plans, select vendors, interpret genetic data in clinical contexts, and support reverse translational research to inform target validation and patient stratification. Requirements: PhD, MD, PharmD, or equivalent in human genetics, with 8+ years of experience, including 4+ years in industry supporting clinical programs, with strong expertise in genomics, genetic testing, data analysis, and regulatory considerations. High-Value: involvement across multiple therapeutic areas, supporting biologics or small molecules, with a focus on clinical trial design, genomic data interpretation, and pharmacogenomics. Collaboration: partner with cross-functional teams, including research, clinical, and regulatory, reporting to the Head of Human Genetics. Work Setup: not specified, but implied to be within a research and development environment with an industry focus.