Manager, Clinical Risk Management
Johnson & Johnson Innovative Medicine
October 2, 2026
Full-time
Remote friendly (Titusville, NJ)
Worldwide
Clinical Research and Development
Role: Manager, Cross Therapeutic Area Clinical Risk Management within R&D Quality at Johnson & Johnson, focusing on identifying, assessing, and mitigating quality risks in clinical trials across multiple therapeutic areas. Responsibilities: Collaborate with trial teams to oversee risk management activities, develop and review Clinical Quality Plans, conduct risk monitoring, facilitate inspections, and support investigations and CAPA development. Ensure trial compliance, inspection readiness, and data integrity throughout the clinical development process.
Qualifications: Bachelor’s degree in a scientific or medical discipline; at least 8 years of experience in healthcare or pharma, with proven GCP and clinical trial quality expertise. Strong communication, project management, and cross-cultural collaboration skills are required. Proficiency in MS Office, with preferred experience in risk management fundamentals, ICH guidelines, GMP/GLP/GPvP, inspection experience, data analytics tools, and knowledge of digital health and real-world evidence.
High-Value: Focus on clinical trial quality assurance in a regulated pharma environment, supporting global multi-country trials, with up to 10% travel expected. The role is based at multiple U.S. and international locations, emphasizing inspection readiness, risk oversight, and compliance with regulatory standards (FDA, EMA). The position offers a salary range of $102,000–$177,100, with benefits aligned with Johnson & Johnson policies.
Qualifications: Bachelor’s degree in a scientific or medical discipline; at least 8 years of experience in healthcare or pharma, with proven GCP and clinical trial quality expertise. Strong communication, project management, and cross-cultural collaboration skills are required. Proficiency in MS Office, with preferred experience in risk management fundamentals, ICH guidelines, GMP/GLP/GPvP, inspection experience, data analytics tools, and knowledge of digital health and real-world evidence.
High-Value: Focus on clinical trial quality assurance in a regulated pharma environment, supporting global multi-country trials, with up to 10% travel expected. The role is based at multiple U.S. and international locations, emphasizing inspection readiness, risk oversight, and compliance with regulatory standards (FDA, EMA). The position offers a salary range of $102,000–$177,100, with benefits aligned with Johnson & Johnson policies.