Manager, RBQM

Role: Support clinical trial quality management through risk-based approaches, focusing on patient safety, data integrity, and compliance. Responsibilities: assist with risk assessments, develop and maintain risk management plans, contribute to centralized monitoring setup and review, support oversight activities, and promote continuous quality improvement and training. Requirements: Bachelor's degree in life sciences or related field; at least 6 years in clinical research or operations, with 1+ year exposure to risk management or RBQM; knowledge of GCP, ICH guidelines, and clinical systems; strong organizational and communication skills; willingness to travel up to 20%. HighValue: RBQM, risk assessments, centralized monitoring (e.g., CluePoints), clinical trial oversight, compliance, GxP, cross-functional collaboration. WorkSetup: not specified, but involves collaboration with study teams, CROs, and quality functions.