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Junior Clinical Trials Data Specialist

Tempus AI · IL · Remote available · Full time

Posted May 21, 2026 · We last checked this listing on Oct 6, 2026

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Likely interview questions for this role

Written from this job description, not a generic list. Each one notes what the interviewer is really checking.

About your past

Tell me about a time you had to keep work accurate while priorities kept changing.

What they are checking: Whether they stay careful when workflows shift, since a wrong trial match wastes clinician time and patient hope.

Describe a project where you worked with people from very different backgrounds, like scientists and product staff.

What they are checking: Whether they can communicate across teams, since reports here are built with scientists, pathologists and product developers.

How do you check your own work before a report goes out?

What they are checking: Whether they have a real self-review habit rather than relying on someone else to catch errors.

Why are you interested in clinical trial matching, and what do you hope to learn in this role?

What they are checking: Whether they understand what the work involves day to day and want to grow in it.

What would you do

You find two sources in the record that disagree about a patient's cancer stage. What do you do?

What they are checking: Whether they flag conflicts and look for the most reliable source instead of quietly picking one.

The posting mentions flexible hours. How do you feel about shifts that change based on business needs?

What they are checking: Whether they have honestly thought about the schedule, since flexibility is a stated requirement of the job.

What would you do if you weren't sure whether a patient met an eligibility criterion?

What they are checking: Whether they ask for help on gray areas instead of guessing, which matters in an entry-level clinical role.

About the work

Walk me through how you'd read a patient's clinical record to decide whether they might match a clinical trial.

What they are checking: Whether they can pull diagnosis, stage, prior treatment and biomarkers out of messy records and compare them to criteria.

A trial requires a specific mutation and no prior immunotherapy. What would you look for in the record to confirm both?

What they are checking: Whether they know where molecular results and treatment history usually live and read eligibility criteria carefully.

How would you explain the difference between a germline and a somatic variant to a coworker who's new to genetics?

What they are checking: Whether their biology background is solid and they can explain it simply to non-specialists.

Practice this interview out loud.

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The full job description

As published by Tempus AI.

Passionate about precision medicine and advancing the healthcare industry? 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. Responsibilities: • Review patient clinical records and use relevant data to determine clinical trial matches. • Independently manage clinical trial workflows, adapting to changing priorities and business needs to ensure efficiency and consistency. • Work collaboratively with cross-functional teams at Tempus (including scientists, pathologists, and product development) to create customized clinical reports. • Navigate and synthesize information from multiple data sources and systems. • Ensure clinical reports are accurate, clear, and aligned with requirements. • Support ongoing and future projects within the team. • Contribute to a dynamic work environment by maintaining flexibility and responsiveness to shifting workflows. • Other duties as assigned. Qualifications: • Bachelor's or Master's degree in Genetics, Molecular Genetics, Cancer Biology, or Biological Sciences. • Willingness to work flexible hours and adapt to business needs. • Strong written and verbal communication skills. • Proficient in critical thinking, interpersonal, and problem-solving abilities. • Ability to manage complex tasks efficiently under time constraints. • Highly detail-oriented with a commitment to accuracy and consistency. • Self-motivated and able to thrive independently as well as within a collaborative, high-performing team. • Demonstrated passion for making an impact in a fast-paced, mission-driven environment. Preferred Qualifications : • Experience reviewing hematology/oncology clinical records. • Experience in critically evaluating clinical trials. • Basic knowledge of generative AI. CHI: $46,000-$50,000 The expected salary range above is applicable if the role is performed from Illinois and may vary for other locations (California, Colorado, New York). Actual salary may vary based on qualifications and experience. Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and other benefits depending on the position. We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

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