Junior Clinical Trials Data Specialist
Tempus AI
About the Role
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.
Key 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.
Requirements & Tech Stack
- 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.