Job Description

Clinical Data Analytics & Reporting LeadAt 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:\xc2\xb7 Responsible for planning, coordination, oversight, and execution of team activities as appropriate and provides technical and project specific guidance to team members.\xc2\xb7 Partner with business representatives to translate requirements for clinical data and reporting/visualization solutions.\xc2\xb7 Hands-on programming and data manipulation for all aspects of data quality and clinical safety review reports/visuals & dashboards.\xc2\xb7 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.\xc2\xb7 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.\xc2\xb7 Serve as primary report/visualization delivery contact for stakeholders.\xc2\xb7 Provide operational oversight and project management of programming activities across multiple trials for assigned portfolio ensuring effective partnership with key stakeholders as appropriate.\xc2\xb7 Lead, organize and proactively engage in project team meetings and develop detailed plans as applicable.\xc2\xb7 Serve as a departmental resource in areas of technical, scientific, disease or therapeutic area expertise.\xc2\xb7 Contribute to and/or lead departmental innovation and process improvement projects.\xc2\xb7 Train, mentor, and coach, and may delegate work.\xc2\xb7 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.QualificationsQualifications\xc2\xb7 Bachelors degree in Computer, Data or Life Sciences or equivalent work experience is required; Masters degree preferred.\xc2\xb7 6+ years of relevant experience in pharmaceutical industry is desired, experience in other industries in Programming role will also be considered.\xc2\xb7 In-depth knowledge of protocol, current clinical drug development processes preferred.\xc2\xb7 In-depth knowledge of data structures and relevant programming languages for data manipulation and reporting. SAS, R, Python, or equivalent programming languages is strongly preferred.\xc2\xb7 Strong knowledge of complex finding data types, including but not limited to biomarker, digital data such as ECG, imaging, etc. a plus.\xc2\xb7 Experience utilizing tools intended for report writing, analytics, visualizations, or dashboard creation (i.e., Spotfire, Tableau, Qlik, JReview, Business Objects, Oracle BI, or Crystal Reports) is strongly preferred.\xc2\xb7 Demonstrated understanding of CDISC requirements and implementation guidelines is preferred, able to consume and translate CDISC standard datasets or similar.\xc2\xb7 Experience in planning and coordinating one or more team activities is preferred.\xc2\xb7 Project management skills and knowledge of team management principles are required.\xc2\xb7 Demonstrated written and verbal communication skills are required.\xc2\xb7 Aptitude and motivation to learn modern technologies and make appropriate recommendations for consideration is preferred.\xc2\xb7 Vendor management oversight experience is required.Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

Johnson & Johnson