Junior Clinical Trials Data Specialist

Passionate about making a difference in the world of cancer genomics?

Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus’ proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time. 

With the advent of genomic sequencing, we can finally decode and process our genetic makeup. We now have more data than ever before but providers don’t have the infrastructure or expertise to make sense of this data. We’re on a mission to connect an entire ecosystem to redefine how genomic data is used in clinical settings. We are looking for a Jr. Clinical Trials Data Specialist who will work with our cross-functional teams on clinical and research initiatives. 

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

Qualifications:

• 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. 

Preferred Qualifications:

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

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