Junior Clinical Trials Data Specialist
Tempus Open At a glance
Junior role at Tempus. Remote, United States · full-time · $46,000–$50,000 base.
remoteroles summary, based on the employer's posting.
What you'll do
- Review patient records and use clinical details to identify trials that may be a match
- Run trial-related workflows independently, adjusting priorities to keep work efficient and consistent
- Bring scientists, pathologists and product development colleagues together to prepare tailored clinical reports
- Combine information from multiple sources and systems, then check reports for accuracy and clarity
- Pitch in on current and upcoming team projects as workflows shift
What you bring
- A bachelor's or master's degree in genetics, molecular genetics, cancer biology or another listed discipline
- Strong written and spoken communication, with careful attention to accurate and consistent work
- You can manage complex assignments under time pressure and work independently as well as with a team
Who this fits
This junior role suits someone who wants to apply biological training to clinical trial matching and reporting. It is remote in the United States, and you need to be willing to work flexible hours as business needs change.
From the employer
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.
Unites States Range: $46,000-$50,000
The expected salary range may vary for other locations. 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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