Junior Clinical Trials Data Specialist
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.
Apply To This Job
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.
Apply To This Job