Manager, Clinical and Safety Analytics

Working with Us Challenging. 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. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us. 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 & Clinical Analytics. Position Responsibilities ● Responsible 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 Spotfire, 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 ● Develop, Run and maintain reports and studies regarding Real world data analytics and present the outcomes to the stakeholders. Other tasks ● Provide scheduled and ad-hoc reports to the leadership team as required ● Supporting Audit Activities related to BMS REMS & Clinical programs. Experience Requirements ●BS/BA degree required, understanding of FDA Risk Evaluation and Mitigation Strategies (REMS) regulations, analytical reporting, and at least 5 - 8 years of relevant pharma/biotech experience. Master’s or advanced degree preferred Key Competency Requirements ● Strong PowerPoint and Excel Skills ● Programming languages like SAS, SQL or Python etc. ● Strong knowledge and expertise in Tableau & and familiarity with Spotfire ● Databases (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 ● Familiarity and ability to navigate with Clinical and Real-world data ● Knowledge of Validation processes and associated...