Junior Clinical Trials Data Specialist

Benefits

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
• •**** Experience reviewing hematology/oncology clinical records
• •Experience in critically evaluating clinical trials
• •Basic knowledge of generative AI.CHI: $46,000-$50,000
• •8 more items(s)

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
• •5 more items(s)