Manager, Clinical and Safety Analytics

As an Analyst at Bristol Myers Squibb, you will be responsible for enhancing and developing a framework related to data analytics reporting within the Worldwide Patient Safety & PV CoE Analytics function. Your key responsibilities will include: - Ensuring compliance with regulatory requirements and enhancing drug safety through qualitative and quantitative research projects - Collaborating with cross-functional teams to analyze data trends from Regulatory, Medical & Clinical Safety, Commercial, and Brand Marketing departments - Maintaining and developing programming, reporting, and analytics applications in BMS environments such as Spotfire, Tableau, and Excel - Utilizing data analysis tools to aggregate and analyze data for actionable recommendations and to answer key business questions - Developing, running, and maintaining reports regarding activities, outcomes, and trends - Remaining informed about the healthcare industry's changing landscape and its impacts on REMS programs and reporting mechanisms - Analyzing key stakeholder complaints, addressing them rapidly, and proposing realistic solutions - Interpreting and contextualizing analytical findings documented by the REMS Advisor team - Running and maintaining reports and studies on Real-world data analytics In addition to the above responsibilities, you will also be expected to: - Provide scheduled and ad-hoc reports to the leadership team - Support Audit Activities related to BMS REMS & Clinical programs Qualifications required for this role: - BS/BA degree - Understanding of FDA Risk Evaluation and Mitigation Strategies (REMS) regulations - 5-8 years of relevant pharma/biotech experience - Masters or advanced degree preferred Key competencies required for this role include: - Strong PowerPoint and Excel Skills - Programming languages like SAS, SQL, or Python - Expertise in Tableau and familiarity with Spotfire - Ability to organize and curate data - Analytical and strategic thinking skills - Knowledge of Clinical and Real-world data - Strong project management and communication skills - Ability to collaborate with cross-functional partners - Strong work ethic and integrity If this role intrigues you and aligns with your interests, even if it doesn't perfectly match your resume, we encourage you to apply. Bristol Myers Squibb offers challenging and meaningful work that can transform both your career and the lives of patients. As an Analyst at Bristol Myers Squibb, you will be responsible for enhancing and developing a framework related to data analytics reporting within the Worldwide Patient Safety & PV CoE Analytics function. Your key responsibilities will include: - Ensuring compliance with regulatory requirements and enhancing drug safety through qualitative and quantitative research projects - Collaborating with cross-functional teams to analyze data trends from Regulatory, Medical & Clinical Safety, Commercial, and Brand Marketing departments - Maintaining and developing programming, reporting, and analytics applications in BMS environments such as Spotfire, Tableau, and Excel - Utilizing data analysis tools to aggregate and analyze data for actionable recommendations and to answer key business questions - Developing, running, and maintaining reports regarding activities, outcomes, and trends - Remaining informed about the healthcare industry's changing landscape and its impacts on REMS programs and reporting mechanisms - Analyzing key stakeholder complaints, addressing them rapidly, and proposing realistic solutions - Interpreting and contextualizing analytical findings documented by the REMS Advisor team - Running and maintaining reports and studies on Real-world data analytics In addition to the above responsibilities, you will also be expected to: - Provide scheduled and ad-hoc reports to the leadership team - Support Audit Activities related to BMS REMS & Clinical programs Qualifications required for this role: - BS/BA degree - Understanding of FDA Risk Evaluation and Mitigation Strategies (REMS) regulations - 5-8 years of relevant pharma/biotech experience - Masters or advanced degree preferred Key competencies required for this role include: - Strong PowerPoint and Excel Skills - Programming languages like SAS, SQL, or Python - Expertise in Tableau and familiarity with Spotfire - Ability to organize and curate data - Analytical and strategic thinking skills - Knowledge of Clinical and Real-world data - Strong project management and communication skills - Ability to collaborate with cross-functional partners - Strong work ethic and integrity If this role intrigues you and aligns with your interests, even if it doesn't perfectly match your resume, we encourage you to apply. Bristol Myers Squibb offers challenging and meaningful work that can transform both your career and the lives of patients.