Manager, Clinical and Safety Analytics

3 days ago

Hyderabad, India Bristol Myers Squibb Full time
Working with UsChallenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.BMS Hyderabad is an integrated global hub where our work is focused on helping patients prevail over serious diseases by building sustainable and innovative solutions. This important science, technology, and innovation center will support a range of technology and drug development activities that will help us usher in the next wave of innovation.Position Summary:This position is responsible for enhancing and developing a framework related to data analytics reporting utilizing metrics collected within the Worldwide Patient Safety & PV CoE Analytics function. The Analyst will enable analytical use of the compliance data that provides insights related to productivity, efficiency, and quality to facilitate informed decision making for BMS REMS Analytics.Position ResponsibilitiesResponsible for ensuring compliance with regulatory requirements, enhancing drug safety and regulatory adherence with qualitative and quantitative research projects through collaboration with data trends from cross-functional teams (Regulatory, Medical & Clinical Safety, Commercial, Brand Marketing, etc.)Maintain and develop programming, reporting and analytics applications in BMS environments such as Tableau, Excel.Leverage internal data systems and tools to efficiently maintain data visualization, communications and reporting processes to minimize manual data retrieving.Utilize data analysis tools to aggregate and analyze data to make actional recommendations and answer key business questions.Develop, Run, and maintain reports regarding activities, outcomes, and trends and be prepared to deliver presentations to management team on a regular and ad-hoc basis.Continually remain apprised of the constantly changing landscape of the healthcare industry and any impacts it may have to our REMS programs and reporting mechanisms.Obtain a deep understanding of the prescriber and pharmacy operating environments through View Job Posting Details vendor and consulting interactions, stakeholder discussions, conference attendance, BMS events etc.Analyze key stakeholder complaints, address rapidly, and discuss with applicable functional leads to collaborate and propose impactful and realistic solutions.Interpret and contextualize analytical findings documented by the REMS Advisor team.Other tasksProvide scheduled and ad-hoc reports to the leadership team as required.Supporting Audit Activities related to BMS REMS programs.Training & Change ManagementIn partnership with WWPS members, develop and execute change management and change readiness assessments and strategies.Support Stakeholder analysis and mapping, identifying potential impacts/risks Manage efforts related to communication and education of the user community on system progress, objectives, and requirements; and develop means to evaluate and ensure organizational readiness.Contribute to initiatives to develop employees’ understanding and acceptance of impacts on specific job roles, policies, technology impacts and business practices.Identify and anticipate organizational challenges and/or resistance; contribute to the development of risk mitigation plans.Plan and Support activities to plan, design, and execute end-user training strategies.Support evaluation of instructional approaches for reports and their requisite systems Conduct and support train-the-trainer workshops as appropriate, related to various reporting applications.Support the review of end-user training materials, job aids and other materials for consistency and relevance in relation to agreed-upon training objectives.Degree RequirementsS/BA degree required, understanding of FDA Risk Evaluation and Mitigation Strategies (REMS) regulations and at least 4 - 8 years of relevant pharma/biotech experience. Master’s or advanced degree preferred.Key Competency RequirementsStrong PowerPoint and Excel SkillsProgramming languages like SAS, SQL or Python etc.Strong knowledge and expertise in TableauDatabases (Salesforce, Postgres, Oracle, SharePoint List etc.)Ability to organize/curate data and see big picture from scattered pieces of information.Analytical and strategic thinking skills required.Knowledge of Validation processes and associated documentationExcellent verbal, writing, presentation and project management skillsStrong strategic orientation with ability to translate into operational priorities and plans.Demonstrated ability to work on multiple projects.Strong willingness to collaborate with cross-functional partners, flexible team member with positive attitude, friendly demeanor, ability to prioritize projects and balance competing priorities.Confidentiality and integrity are required.Strong work ethic a must

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