Senior Manager, Real World Evidence Analyst Starszy Manager ds. Analityki Rzeczywistych Dowodów (Real World Evidence RWE)

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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: Senior Manager Real World Evidence Analyst - Starszy Manager ds. Analityki Rzeczywistych Dowodów (Real World Evidence - RWE) - based in Warsaw - is a key member of cross-functional teams and RWE-CoE within GBDS. This role will perform the curation transformation and analysis of complex healthcare datasets to inform evidence generation support developing clinical program design clinical trial execution and other data-driven decision-making addition the RWE Analyst will be supporting in-house real-world evidence (RWE) trials to generate insights that enhance clinical and regulatory strategies. The ideal candidate will have deep expertise in working with RWD (e.g. claims EMR registries) RWE trials experience strong analytical and communication capabilities and a collaborative mindset.

Key Responsibilities:

• Curate and assess the quality of real-world data (RWD) assets to ensure their suitability and understanding for intended use.

• Design and implement data pipelines to transform raw RWD into datasets ready for analysis.

• Collaborate with cross-functional teamsincluding Biostatistics Data Science HEOR Epidemiology/Safety Clinical and ITto define data requirements and analytical strategies.

• Conduct exploratory data analyses identify patient cohorts and perform data summary analytics to support real-world evidence (RWE) generation.

• Participate in the design of RWE studies including the development of methodologies data analysis interpretation and reporting of study results.

• Author or review study documents such as protocols statistical analysis plans study reports publications and study-level specifications.

• Develop and maintain documentation detailing data sources transformations and analytical methods.

• Ensure all work complies with data governance privacy and regulatory standards.

• Stay up to date with industry and regulatory trends tools and best practices in RWD/RWE analytics.

• Continually expand technical knowledge of statistical considerations in real-world evidence generation to ensure high-quality study design and analysis.

• Enhance understanding of the drug development process as well as regulatory and commercial requirements.

Qualifications & Experience:

• Masters or PhD in Epidemiology Biostatistics Data Science Health Informatics or a related field.

• 3 years of experience working with real-world healthcare data (claims EMR registries etc.).

• 2 years of experience in pharmaceutical industry (e.g. Pharma CRO Biotech) and clinical trials.

• Proficiency in SAS R Python or similar tools for data manipulation and analysis. AI/ML knowledge is a plus.

• Good verbal and written communication skills in English

• Good understanding of industry RWD vendor database.

• Experience with RWD data curation engineering exploration and quality control in large-scale datasets.

• RWD trial design and analysis experience

• Ability to communicate complex real-world data concepts to non-technical stakeholders.

• Ability to work successfully within cross-functional teams

• Ability to organize multiple work assignments and establish priorities

• Strong understanding of healthcare industry regulatory compliant data standards.

• Good understanding of regulatory requirements & clinical trial design is preferred.

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If you come across a role that intrigues you but doesnt perfectly line up with your resume we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

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With a single vision as inspiring as Transforming patients lives through science every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture promoting global participation in clinical trials while our shared values of passion innovation urgency accountability inclusion and integrity bring out the highest potential of each of our colleagues.

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Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles onsite presence is considered an essential job function and is critical to collaboration innovation productivity and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

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