A global healthcare leader, Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented and performance driven people. All of which makes them one of the most rewarding employers in their field.
Post: Principal Analyst-Analytics
Responsible for leading user requirement gathering for complex reports for data review and analysis. Independently manage requirements gathering and implementation of complex reports. Provide quantitative analytical support and produce key reports for Oncology Global Development, including BDM, GMO and GPTs. These tasks are to be performed independently. Drive the implementation of data analytics reports for optimal data review by working with the users to establish robust user specification and with programmers to implement the optimal output. Proactively identify or address needs for optimal data review reports working with users and programmers as appropriate.
Implement project plans for delivery, ensuring customer needs are addressed in a timely manner within Oncology Development Drive development of appropriate user training. Drive all necessary change management activities related to implemenation of new data review tools / reports as related data cleaning, review and visualization. Provide understandable and actionable reports on clinical data and monitoring of clinical data for key stakeholders Provide quantitative analytical support to the global program teams, including providing support on analyzing reports Systematically sample / monitor utilization of reports and tools, perform and coordinate periodic review of outputs.
Report findings and take necessary steps to ensure reports are being for optimal data review. Work with the internal SMEs and key stakeholders in providing analysis and interpretation of clinical program/trial operational data Lead initiatives within Analytics, including training, to support overall compliance and adherance to data review through robust reports and tools. Proactively identify and address areas of concerns to avoid issues and ensure consistency, accurancy and completeness of reported clinical data.
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Candidate Profile: Masters/Bachelor’s Degree in Life Science or similar field. Fluent English (Oral and Written)
•Minimum 6 years’ experience in Business Analytics and/or Clinical Trial Management
•Pharma, CRO, Life Science experience of 4 years would be preferred. •Total experience of at least 7 years is preferred. Required skills:
•Good quantitative & systems background.
•Ability to translate technical concepts for non-technical users in the areas of clinical databases (both internal and external).
•Familiarity with Business Intelligence tools including, Cognos, Hyperion, Crystal Reports, Spotfire, Jreview
•Ability to provide innovative solutions
•Ability to program in Microsoft Excel
•Ability to produce professional PowerPoint Slides that clearly communicate analyses to stakeholders
•Attention to detail, quality, time management and customer focus
•Ability to work independently, in teams, under pressure, demonstrating initiative and flexibility through effective and innovative technical ability. •Interpersonal and communication skills, ability to operate effectively in a matrix environment. Desired skills:
•Good understanding of Clinical Development and Operational process and regulatory requirements is preferred
•Solid understanding of Clinical Trial and Database Management systems for clinical research and development would be an added advantage
•Understanding trends in global clinical development, including key competitors
•Good knowledge of SAS/R/Minitab/S+ preferred
Experience: 6-7 Years
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: Development & Medical
Job Type: Full Time
Employment Type: Permanent
Job ID: 131362BR
End Date: 20th Dec., 2013
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