Associate Director- Clinical Data Standards

Role Overview: As a Clinical Data Standards Specialist at Novartis, you will strategically and tactically support the Director of Clinical Data Standards. Your responsibilities will include advising and leading the planning, development, and implementation of Industry compliant clinical data standards, infrastructure, and automation technologies. You will provide expert support to business users and teams on various aspects including data standard collection tools, data transfer specifications, analysis data standards, and automation solutions. Additionally, you may lead global teams to ensure alignment with the CDS strategy and drive efficient implementation of new standards and technologies. Key Responsibilities: - Ensuring alignment with the CDS strategy - Responsible for Clinical Data Standard/automation solution planning, development, and support - Serving as the primary contact for global / TA data standards and technologies - Driving efficient and timely implementation of new standards and technologies - Leading technical review and assessment of industry and regulatory standards - Contributing to the development, maintenance, and training of clinical standards systems - Acting as an expert consultant providing Clinical Data Standards input to relevant areas - Mentoring and providing technical guidance to Clinical Data Standards associates Qualifications Required: - Work experience in managing crises, functional breadth, project management, and collaborating across boundaries - Skills in automation, biostatistics, clinical trials, computer programming, data analytics, decision making, metadata management, and statistical analysis - Proficiency in English language,