Junior Clinical Trials Data Specialist

Tempus AI; Springfield (IL); Vor Ort; USD 46.000 - 50.000; Vollzeit

Zusammenfassung

Tempus AI is seeking a detail-oriented professional to review patient clinical records and determine clinical trial matches. You will manage clinical trial workflows, collaborate with scientists, pathologists, and product teams, and synthesize information from diverse data sources to produce precise clinical reports.

The role emphasizes flexibility, accuracy, and the ability to thrive in a fast-paced, mission-driven environment with the potential for meaningful impact on patient care.

Qualifikationen

• Bachelor's or Master's degree in Genetics, Molecular Genetics, Cancer Biology, or Biological Sciences.
• Strong written and verbal communication skills.
• Highly detail-oriented with accuracy and consistency.
• Self-motivated and able to thrive independently or in a team.

Aufgaben

• Review patient clinical records and determine clinical trial matches.
• Independently manage clinical trial workflows with changing priorities.
• Collaborate with cross-functional teams to create customized clinical reports.
• Navigate and synthesize information from multiple data sources and systems.
• Ensure clinical reports are accurate and align with requirements.
• Support ongoing and future projects within the team.
• Maintain flexibility and responsiveness to shifting workflows.

Kenntnisse

Genetics background

Strong communication

Critical thinking

Time management

Independent worker

Ausbildung

Bachelor's or Master's in Genetics or Biological Sciences

Jobbeschreibung

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.

Location & Salary

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.

Equal Opportunity

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.