Remote Junior Clinical Trials Data Specialist

Summary

Join our team as a Jr. Clinical Trials Data Specialist to work collaboratively within cross-functional teams at Tempus, creating customized clinical reports, analyzing patient records, and supporting ongoing projects.

Requirements

• Minimum of a BS degree in Genetics, Molecular Genetics, Cancer Biology, or Biological Sciences
• Willingness to be flexible
• Ability to learn new skills quickly and adapt to new processes smoothly
• Excellent communication skills with the ability to work both independently and in a group setting
• Excitement and drive to make a difference in a fast-paced energetic work environment

Responsibilities

• Works collaboratively within cross-functional teams at Tempus (including but not limited to scientists, pathologists, product development, etc.) to create customized clinical reports
• Analyze patient clinical records and molecular testing results to identify potential clinical trials
• Perform critical quality control functions in clinical report workflow
• Support ongoing and future projects within the team
• Ability to quickly adjust priorities according to workflow or business needs

Preferred Qualifications

• Hematology/oncology knowledge
• Experience reading and critically evaluating clinical trials