TA Director, Risk Management Lead - Multiple Therapeutic Areas (Hybrid)

Role: TA Director of Risk Management leads risk strategies and practices across immunology, neuroscience, and aesthetic therapeutic areas in clinical development. Responsibilities include driving portfolio-level risk identification and mitigation, supporting protocol design with critical-to-quality elements, developing and mentoring a team of risk leads, overseeing risk insights and dashboards, managing RAMP processes, and collaborating with cross-functional stakeholders to embed risk-based quality practices. Qualifications: Bachelor's degree in life sciences or related field; 15+ years in clinical research or operations, with at least 5 years in leadership; expertise in risk-based quality management, GCP, and regulatory guidelines; experience with risk assessments, RAMP, and risk-based modifications; professional risk management certifications preferred. High-Value: Focus on risk management in clinical trials within immunology, neuroscience, and aesthetics, with emphasis on data-driven decision-making, regulatory compliance, and cross-functional collaboration. Work Setup: Hybrid on-site in Lake County, IL or Irvine, CA, working onsite T-TH, with local candidates preferred.