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 50% onsite work, 4+ years of experience, proficiency in SQL, Python, and Tableau, and biopharma experience preferred.
🌎 - Country
United States
💱 - Currency
$ USD
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💰 - Day rate
536
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🗓️ - Date
January 8, 2026
🕒 - 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
Lawrenceville, NJ
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🧠 - Skills detailed
#Python #R #Data Quality #"ETL (Extract #Transform #Load)" #SQL (Structured Query Language) #Data Analysis #Tableau #Regression #Visualization #Statistics
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 descriptio n:Summary: 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 activitie s.Roles & Responsibilitie • s:Collaborates and works closely with cross-functional teams, including data analysts/engineers and business stakeholders, to understand their needs and gather requirement • s.Cleans, transforms and pre-processes data to ensure data quality, consistency and compatibility for analysi • s.Develops and implements data analysis plans to answer clinical and safety question • s.Applies analytical and/or statistical techniques to analyze data and generate insights on safety question • s.Visualizes data and results to share insights with technical and non-technical cross-functional stakeholder • s.Interprets and communicates findings through reports, presentations and visualization • s.Stays up to date and compliant with the regulatory landscape related to drug safety and data analyse • s.Works closely with PV CoE and other stakeholders, sharing knowledge and best practices within the broader safety and analytics team s.Skills & Competencie • s:Strong understanding of data sources, such as clinical trial data, electronic health records, and other healthcare database • s.Proficiency in data pre-processing, cleaning and transformation techniques to ensure data quality and compatibility for analysi • s.Knowledge of relevant analytical and statistical methodologies, such as regression analysis, survival analysis et • c.Excellent problem-solving skills and the ability to derive meaningful insights from complex real-world data set • s.Excellent communication and presentation skills to effectively convey complex concepts and finding • s.Ability to work collaboratively in cross-functional teams and manage multiple projects simultaneousl • y.Strong attention to detail and accuracy in data analysis and interpretatio n.Experienc • e:4+ years of Data Analyst experien • ceIntermediate to Advanced skills with Tableau or Ql • ikExtensive experience with SQL and Python or R or S • ASStrong communication skil • lsBiopharma experience preferr • edBachelors or Masters (preferred) degree in a relevant field, such as Biostatistics, Analytics, Engineering or related disciplin e.