As the industry’s leading cardiovascular contract research organization, at the heart, we are a team of dedicated scientists with a passion for helping our clients answer their drug discovery, cardiovascular toxicology and safety pharmacology questions.

Current Openings

Small Animal Surgeon

The Small Animal Surgeon will be primarily responsible for conducting in vivo small species surgical procedures, as well as collecting and analyzing data from these examinations.


The primary responsibility for this position is to generate high-quality data from small species in vivo procedures, focusing on the conduct of cardiovascular safety pharmacology and toxicology studies. Previous in vivo small species experience is a must, as well as desire to conduct novel procedures as well as established models within cardiovascular research.

This full time position offers excellent benefits and a competitive salary structure and will be at our Chicago location. There is no remote work option for this position.


  • B.S. in biomedical field with extensive surgical experience
  • Strong knowledge of cardiovascular physiology and safety pharmacology studies used to investigate potential cardiac liabilities
  • Ability to analyze, interpret, and summarize moderately complex data sets
  • Working knowledge of Microsoft Excel and Word
  • Attention to accuracy and detail


  • M.S., Ph.D., M.D. in biomedical field
  • Experience with nonclinical echocardiography desirable

To apply for this position or receive more information, please contact

Report Writer

The Report Writer will be responsible for supporting the development of high-quality client reports by assisting with QC/QA of data and generating quality interpretation of these complex results.

  • Review study protocols and amendments as pertaining to data analysis and interpretation for reporting
  • Verify findings and consult with the Study Director and QA lead regarding any abnormalities
  • Generate high-quality client reports, focusing on the interpretation of cardiovascular drug discovery and toxicology data
  • Create report-ready tables, format data sets and collate all supporting documentation into report framework
  • Assist QA team with QC analysis on both exploratory and GLP studies

This role could be full or part time (hours negotiable) with remote location option.


  • B.S. in Biological Sciences or related Medical Science field
  • Advanced writing competency and exceptional organizational skills
  • Strong proficiency in Microsoft Excel and Word
  • Attention to accuracy and detail
  • Ability to work independently to meet expected timelines while providing accurate, scientifically sound analysis for both exploratory and GLP studies
  • Ideal candidate with 1-3 years of work-related experience preferably as a medical writer, manuscript editor or as a QA associate

To apply for this position or receive more information, please contact