JOB TITLE: Clinical Safety Analytics Associate
Location: Lawrenceville, NJ (50% on-site)
Duration: 6 months initial (potential extension/potential right to hire)
Must Have List:
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
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.
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
• Bachelor's or Master's (preferred) degree in a relevant field, such as Biostatistics, Analytics, Engineering or related discipline.
• Minimum of 3-5 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
If hired, you will enjoy the following Eclaro Benefits:
- 401k Retirement Savings Plan administered by Merrill Lynch
- Commuter Check Pretax Commuter Benefits
- Eligibility to purchase Medical, Dental & Vision Insurance through Eclaro
If you feel you are qualified with the required skills and if you are interested, please free to send your word version most updated resume TAILORED to the job description above to June@eclaro.com or call (212)804-7476.
Equal Opportunity Employer: Eclaro values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
