Prolacta Bioscience-posted 8 months ago
$140,000 - $160,000/Yr
Full-time • Senior
Remote • Orangeburg, SC
Chemical Manufacturing

Do you want to contribute to a larger purpose to save the lives of infants in the NICU? This is Prolacta Bioscience's mission! Take a look at this opportunity with our IT team, which is seeking a passionate individual, to fill the role of our Clinical Trial Data Analyst III. This role will research, develop and implement data analysis projects including but not limited to data reporting, data visualizations, and ad-hoc research projects. The ideal candidate will have strong background on handling clinical study data and performing statistical analysis in both the business and clinical study setting. The candidate will achieve this thru using advanced proficiency in SAS or R, and data manipulation using a SQL Server.

  • Collaborate with clinical operations and IT teams to employ effective Clinical Data Management techniques to support clinical trials with sponsor companies.
  • Assist in the analysis of data from clinical studies.
  • Gather, clean, and preprocess data from various sources, including but not limited to transactional SQL server databases, flat files, and MS Excel, following the best ETL practices to make it available for advanced analytics.
  • Create new database objects in SQL Server including, tables, views, stored procedures, and ETL packages to enhance product functionality.
  • Examine data trends and patterns to pinpoint areas for enhancement and provide actionable recommendations to leadership.
  • Employ statistical and machine learning methods to derive insights from data that further enhance Sales growth, Forecasting, Operational Excellence, Marketing and Business Development.
  • Perform statistical analysis and fine-tune models for improved accuracy.
  • Translate complex data into actionable insights for business decisions.
  • Work closely with stakeholders to understand their needs and deliver relevant data-driven solutions.
  • Create clear and compelling visualization of data to communicate findings to both technical and non-technical audiences.
  • Develop dashboards and reports to facilitate data access for team members.
  • Strongly adhere to Prolacta's structured SDLC (software development life cycle) and validation processes.
  • Develop SOPs as needed.
  • MS in Statistics, Computer Science, Data Science, Math or related field with 6+ years of relevant experience, or bachelor's degree in these fields with 8+ years of relevant experience.
  • Experience in developing statistical and machine learning models related to clinical studies using SAS or R.
  • In-depth understanding of statistical techniques and methodologies, along with an understanding of hypothesis testing and A/B testing (such as t-tests and ANOVA).
  • Experience with SQL Server 2008/2014/2016.
  • Experience in SQL capable of writing basic queries from scratch and modifying complex queries.
  • Experience in data management principles.
  • Proven experience in clinical data management best practices.
  • Experience in writing ETL processes in SQL Server.
  • Expertise in data-driven storytelling to create and deliver compelling presentations featuring exceptional visuals using Power BI, Tableau, etc.
  • Familiarity with Ralph Kimball data modeling approach of data warehouse.
  • Experience in FDA regulated drug or healthcare companies desired.
  • Basic understanding of drug development process and regulatory filings.
  • Good oral and written communication skills.
  • Up to 100% healthcare coverage starting on your first day.
  • Discretionary stock options.
  • 401(k) match.
  • Four weeks PTO during your first year of employment.
  • Generous time-off program for new parents.
  • Participation in employee affinity groups.
  • Volunteer time off.
  • Access to different educational opportunities.
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