Risk Surveillance Lead

About The RoleFacilitate trial protocol risk assessment across multiple cross‑functional domains (clinical, operational, data management, vendors, regulatory, etc.) associated to critical‑to‑quality (CtQ) data and processes, including definition of quality tolerance limits (QTLs), evaluation of risks based on likelihood, detectability, impact, and ensuring mitigation strategies / plans are defined.Responsible for drafting, maintaining, and archiving the study‑specific documentation of risk management activities e.g., Integrated Quality Risk Management Plan (IQRMP).Partner with the RBQM system configuration team to ensure risk indicators, quality tolerance limits and other analytics / visualizations are programmed and functioning per operational requirements in the RBQM system.Conduct periodic central surveillance of aggregate data at the study and potentially program level, leveraging available analytics / visualizations in the RBQM system to identify emerging risks and / or issues.Facilitate risk review meetings and discussions with study and potentially program team members to effectively communicate findings, support, and encourage robust root‑cause identification and mitigation strategies.Support and participate in internal and external audits and inspections.Collaborate with training departments to support training initiatives and aid in the adoption of the RBQM approach.Identify and share lessons learned, best practices, successes, case studies, failures, and process improvement opportunities to promote continuous improvement and consistency with RBQM processes.Act as a change agent, champion, subject‑matter expert and point of contact for RBQM methodology, leading study teams to understand and follow best practices to achieve maximum benefit.ExperienceBachelor’s Degree in a health‑related or life science area, or equivalent combination of education, training, and work experience.Minimum of 4 years of experience in the pharmaceutical or CRO industry.Preferred minimum of 1 year of experience in Risk‑Based Quality Management.Robust understanding of the drug development process and clinical trial execution.Knowledge of industry regulatory standards including 21CFR Part11, ICHE6, ICHE8 (GCP).Experience in risk management, sponsor audits and health‑authority inspections, root‑cause analyses and mitigation strategies as well as Corrective Actions Preventive Actions.Knowledge of RBQM IT systems or other data analytic systems.Demonstrated ability to analyze data, identify patterns and make recommendations for improvement.Demonstrated ability to effectively lead cross‑functional team meetings.Experience forming cross‑functional collaborations; strong interpersonal skills.Supports a culture of continual improvement and innovation; promotes knowledge sharing.Ability to influence without authority.Think creatively; challenges the status quo.LanguagesEnglish : fluent written and spoken.Why NovartisHelping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https : / / / about / strategy / people-and-cultureBenefits and RewardsRead our handbook to learn about all the ways we’ll help you thrive personally and professionally : https : / / / careers / benefits-rewards.Seniority levelMid‑Senior levelEmployment typeFull‑timeJob functionOtherIndustryPharmaceutical ManufacturingJ-18808-Ljbffr#J-18808-Ljbffr