Data Analyst

7 days ago

Princeton, United States TSR Consulting Full time
About TSR:

TSR is a relationship-based, customer-focused IT and technical services staffing company.

For over 40 years TSR, Inc. and its wholly owned subsidiary, TSR Consulting Services, have prospered in the Information Technology staffing business, earning the respect of companies both large and small with well refined candidate screening, timely placement, and a real understanding of the right skill sets required by our clients.

Mission & Vision

We do not believe in building a vision around the company but building a company around our vision, which is simply;

Every employee's voice matters, their effort is appreciated, and their talent is rewarded.

We challenge each employee daily, to raise the bar on how we treat our consultants and candidates. For far too long in this industry, candidates have been ghosted, lied to, or placed at a client and then forgotten about. Each day our staff works tirelessly at qualifying and placing, top talent with our clients, in a compassionate and caring manner.

Not every candidate is a match for the job, but every candidate and consultant will be treated with respect and professionalism.

Data Analyst

Job Description

  • Location: Princeton, New Jersey
  • Type: Contract
  • Job #80960
Our client, a leading pharmaceutical company, is hiring a Clinical Safety Analytics Associate, on a contract basis.

Job ID #: 80960

Work Location:
Princeton, NJ - Hybrid, 50% on site

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 activities.

Education/Experience:
  • Bachelor's or Master's (preferred) degree in a relevant field, such as Biostatistics, Analytics, Engineering or related discipline.
  • 3 years of experience in data analysis, statistical modeling, and data visualization, preferably within the biopharma or healthcare industry.
  • Experience applying statistical and analytical techniques, to analyze real world data
  • Experience with Python or R or SAS and SQL required
  • Working knowledge of visualization tools, such as Tableau or Power BI
  • Experience or familiarity with the biopharma industry
Knowledge/Skills:
  • 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
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

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