Senior Principal Clinical Data Standards Specialist

Major accountabilities:

• Drive the implementation of data analytics reports and dashboards for optimal data review by working with the users to establish robust user specifications and with programmers to implement the optimal output -Translate business requirements into logical models and provide direction to the development team to translate business logic.
• Lead authoring of the user requirements document, functional specifications and functional testing scripts -Proactively identify or address needs for optimal data review working with users and programmers as appropriate.
• Implement and execute robust project plans for delivery, ensuring customer needs are addressed in a timely manner.
• Provide coordination between the project resources so that deadlines are met on deliverables.
• Drive development of appropriate user training.
• Drive all necessary change management activities related to implementation of new data review tools / reports as related to data cleaning, review and visualization.
• Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable)

Key performance indicators:

• Timely execution of of projects & data requests -Feedback from project sponsors and key stakeholders -Adherence to Novartis policy and guidelines -Metrics and Adherence to KPIs

Minimum Requirements:

Work Experience:

• Functional Breadth.
• Cross Cultural Experience.
• Managing Crises.
• Collaborating across boundaries.
• Operations Management and Execution.

Skills:

• Automation.
• Biostatistics.
• Clinical Trials.
• Computer Programming.
• Metadata Management.
• Statistical Analysis.

Languages :

• English.

Skills Desired

Automation, Biostatistics, Clinical Trials, Computer Programming, Metadata Management, Statistical Analysis