Associate Director- Clinical Data Standards
Associate Director- Clinical Data Standards
Posted on :
03-06-2025
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1 Vacancy
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Job Description
Band
Level 5Job Description Summary
Strategically and tactically supports Director Clinical Data Standards. Responsible for advising/leading the planning development and implementation of Industry (CDISC and regulatory) compliant high quality clinical data standards infrastructure or automation technologies. Providing expert support and stellar customer focus to business users and teams on their use including: -Data standard collection tools in EDC (CRFs edits checks derivations core configurations) -Data transfer specifications -Analysis data/TFL standards/Define -Automation solutions / technologies -Business infrastructure business rules and guidelines. May lead global teams.Job Description
Major accountabilities:
- Ensuring alignment with the CDS strategy; Responsible for Clinical Data Standard/automation solution planning definition development validation and support
- Serves as the primary contact for global / TA data standards and/or technologies ensuring timely and quality deliverables.
- Responsible for driving efficient high quality and timely implementation of new standards and/or technologies.
- Ensure efficient governance and approval of global clinical data standards / technologies liaising with governance boards as needed.
- Lead the technical review and assessment of industry and regulatory standards and technologies supporting regular gap/impact analysis and implementation of action plans where needed.
- Lead and contribute to the development maintenance and training of relevant clinical standards systems and processes.
- Act as an expert consultant providing Clinical Data Standards input to all relevant areas including electronic data capture/database programming edit check programming report programming electronic data loads IVR technology electronic patient reported outcomes metadata management and/or other clinical data management or analysis data and TFL-related systems.
- Act as primary subject matter expert (SME) for assigned area providing support consultation and training to end users and SME networks on implementation of standards and related tools on development programs.
- Provide mentoring and technical guidance to Clinical Data Standards associates; Contributes to the effectiveness and development of talent.
Key performance indicators:
- Timely execution of of projects and data requests;
- Feedback from project sponsors and key stakeholders
- Adherence to Novartis policy and guidelines -Metrics and Adherence to KPIs
Work Experience:
- Managing Crises.
- Functional Breadth.
- Project Management.
- Collaborating across boundaries.
- Representing the organization.
Skills:
- Automation.
- Biostatistics.
- Clinical Trials.
- Computer Programming.
- Cross-Functional Teams.
- Data Analytics.
- Decision Making Skills.
- Metadata Management.
- Statistical Analysis.
Languages :
- English.
Skills Desired
Automation Biostatistics Clinical Trials Computer Programming Cross-Functional Teams Data Analytics Decision Making Skills Metadata Management Statistical AnalysisRequired Experience:
Director
Employment Type
Full-Time
Key Skills
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