Bristol Myers Squibb

Data Analyst

⭐ - Featured Role | Apply direct with Data Freelance Hub
This role is for a Data Analyst in Lawrenceville, NJ, lasting 6 months at $60.19 - $67.19/hr. Requires 4+ years of experience, proficiency in SQL and Python/R, and biopharma experience preferred. Local candidates must attend an in-person interview.
🌎 - Country
United States
💱 - Currency
$ USD
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💰 - Day rate
536
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🗓️ - Date
December 6, 2025
🕒 - Duration
More than 6 months
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🏝️ - Location
Hybrid
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📄 - Contract
W2 Contractor
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🔒 - Security
Unknown
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📍 - Location detailed
Lawrence, NJ
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🧠 - Skills detailed
#Databases #Regression #Python #Data Quality #Statistics #Visualization #SQL (Structured Query Language) #Tableau #Data Analysis #R #Qlik #"ETL (Extract #Transform #Load)" #SAS
Role description
Job Title: Data Analyst Location: Lawrenceville, NJ 08648 Duration: 6 Months Duration Pay Rate: $60.19 - $67.19/ hr on W2 The candidate must be able to work 50% onsite at Lawrenceville. Local candidates are preferred. The candidate must be able to come in for an onsite, in-person interview as a part of the process. Job description: Clinical Safety Analytics Associate will play a critical role within the PV CoE. This position focuses on assisting with analyzing data and deriving insights from clinical and safety data sources to generate evidence and support decision making across the organization. The Associate will leverage a variety of analytics and visualization techniques to contribute to research, clinical development, drug safety and post-marketing activities. Roles & Responsibilities: • Collaborates and works closely with cross-functional teams, including data analysts/engineers and business stakeholders, to understand their needs and gather requirements. • Cleans, transforms and pre-processes data to ensure data quality, consistency and compatibility for analysis. • Develops and implements data analysis plans to answer clinical and safety questions. • Applies analytical and/or statistical techniques to analyze data and generate insights on safety questions. • Visualizes data and results to share insights with technical and non-technical cross-functional stakeholders. • Interprets and communicates findings through reports, presentations and visualizations. • Stays up to date and compliant with the regulatory landscape related to drug safety and data analyses. • Works closely with PV CoE and other stakeholders, sharing knowledge and best practices within the broader safety and analytics teams. Skills & Competencies: • Strong understanding of data sources, such as clinical trial data, electronic health records, and other healthcare databases. • Proficiency in data pre-processing, cleaning and transformation techniques to ensure data quality and compatibility for analysis. • Knowledge of relevant analytical and statistical methodologies, such as regression analysis, survival analysis etc. • Excellent problem-solving skills and the ability to derive meaningful insights from complex real-world data sets. • Excellent communication and presentation skills to effectively convey complex concepts and findings. • Ability to work collaboratively in cross-functional teams and manage multiple projects simultaneously. • Strong attention to detail and accuracy in data analysis and interpretation. Experience: • 4+ years of Data Analyst experience • Intermediate to Advanced skills with Tableau or Qlik • Extensive experience with SQL and Python or R or SAS • Strong communication skills • Biopharma experience preferred • Bachelors or Masters (preferred) degree in a relevant field, such as Biostatistics, Analytics, Engineering or related discipline.