Senior I Clinical Data Analytics & Reporting Lead - Mumbai/Bangalore/Hyderabad

Clinical Programming: Senior I Clinical Data Analytics & Reporting Lead

At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working to create a world without disease and the development of best-in-industry data science capabilities is critical to our ambition to be most innovative healthcare company.

Within our Clinical & Statistical Programming (C&SP) organization we are looking for experienced individuals with in-depth programming and visualization competencies to join our Clinical Data Analytics & Reporting (CDA&R) team. This is an exciting opportunity to be part of an innovative group that is pivotal in defining our next generation data and visualization strategies.

The Clinical Data Analytics & Reporting Lead, within the CDA&R team, will be responsible for interpretation and translation of clinical data review needs into technical specifications, aggregation of data sources and reporting solutions/visualizations. You will also be responsible for designing and developing technical solutions in support of complex/critical clinical programming, reporting activities, visualization builds and urgent requests. Lastly, you will serve as a delivery contact for stakeholders that could include, but not limited to, risk based central monitoring, data management, clinical scientists/data reviewers, etc.

As required, lead large scale cross-functional projects which require project and stakeholder management skills. Create/develop and improve clinical data safety review and cleaning efficiency by providing innovative and forward-thinking reporting/visualization prototype solutions, report library templates, visualization templates, macros, and other solutions for use cross studies. Provide operational oversight and technical project management of programming and technical activities across multiple trials for assigned areas ensuring effective partnership with key stakeholders as appropriate.

Responsibilities Include:

• Responsible for planning, coordination, oversight, and execution of team activities as appropriate and provides technical and project specific guidance to team members.
• Partner with business representatives to translate requirements for clinical data and reporting/visualization solutions.
• Hands-on programming and data manipulation for all aspects of data quality and clinical safety review reports/visuals & dashboards.
• Design and develop technical solutions in support of complex/critical clinical programming and reporting/visualization activities, including urgent requests at trial or cross-trial levels.
• Apply technical expertise to develop solutions that increase efficiency and quality, macros, report or visualization library templates, solutions for use cross studies for clinical data safety review and cleaning, etc.
• Serve as primary report/visualization delivery contact for stakeholders.
• Provide operational oversight and project management of programming activities across multiple trials for assigned portfolio ensuring effective partnership with key stakeholders as appropriate.
• Lead, organize and proactively engage in project team meetings and develop detailed plans as applicable.
• Serve as a departmental resource in areas of technical, scientific, disease or therapeutic area expertise.
• Contribute to and/or lead departmental innovation and process improvement projects.
• Train, mentor, and coach, and may delegate work.
• Serve as subject matter expert in the field of clinical data analytics/sciences by knowing or learning industry leading tools, researching related technical literature, and attending conferences/training courses.