Description:

The Jr. Clinical Trials Data Specialist will work collaboratively within cross-functional teams at Tempus, including scientists, pathologists, and product development, to create customized clinical reports.
This role involves analyzing patient clinical records and molecular testing results to identify potential clinical trials.
The specialist will perform critical quality control functions in the clinical report workflow.
Support for ongoing and future projects within the team is expected.
The ability to quickly adjust priorities according to workflow or business needs is essential.

Requirements:

A minimum of a BS degree in Genetics, Molecular Genetics, Cancer Biology, or Biological Sciences is required.
Candidates must demonstrate a willingness to be flexible.
The ability to learn new skills quickly and adapt to new processes smoothly is necessary.
Excellent communication skills are required, with the ability to work both independently and in a group setting.
Candidates should possess excitement and drive to make a difference in a fast-paced energetic work environment.

Tempus offers a full range of benefits, which may include incentive compensation and restricted stock units.
Medical and other benefits are also provided, depending on the position.
The expected salary range for this role in Illinois is $45,000—$50,000 USD, with actual salary varying based on qualifications and experience.