Senior Centralized CTL

Join our team as a Senior Centralized Clinical Team Lead, where you will play a key role in ensuring the quality and safety of clinical trials. You will oversee central monitoring activities, risk assessments, and provide technical leadership to ensure compliance with industry standards and regulatory requirements. Key Responsibilities: Review trip reports, identify risks, and communicate trends or safety concerns. Risk review activities at study, site, and regional levels, ensuring proactive risk management. Collaborate with study teams to refine processes, resolve issues, and ensure data-driven decision-making. Provide mentorship and training to team members on monitoring and reporting processes. Support regulatory inspections and ensure inspection readiness. Managing Protocol Deviations and Quality events as per study needs Qualifications: Bachelor's degree in Life Sciences or equivalent; advanced qualifications preferred. Minimum of 10 years of clinical research experience, with 2+ years in trip report review or centralized monitoring. Previous CTL/Lead CRA/management experience. Strong knowledge of ICH-GCP and regulatory requirements. Proficiency in MS Office and risk management tools. Excellent analytical, organizational, and leadership skills.

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