RemoteWLBRemote only
Back to all jobs
Tempus logo
Remote role · assistan

Assistant Director of Clinical Science Oncology

Tempus

SalaryUSD $135,000~$185,000
Role brief

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.

What you’ll do

  • Oversee the operational activities of the Clinical Science team to support a high quality next-generation sequencing workflow with rapid turnaround times
  • Manage a team of genomic scientists and oversee team metrics that align to business objectives.   
  • Ensure delivery of high quality results and regulatory compliance, including FDA, CAP, CLIA, NYS, etc.
  • Plan and direct projects to ensure clinical reports are accurate and to improve operational efficiencies. 
  • Collaborate with diverse roles, including Scientists, Pathologists, Product, Engineering, and Operations to implement solutions for high volume and high growth. 
  • Intentionally foster a workplace culture that is consistent with the clinical team’s guiding principles,Tempus core values and identified vision. 

Preferred Qualifications

  • Higher degree (e.g. Ph.D. or M.D.) in Human Genetics, Molecular Genetics, Genomics or related field
  • Experience managing teams in a high-complexity laboratory or highly regulated environment 
  • Experience leading teams through high growth and rapid change 
  • Demonstrated ability to thrive in a high growth and fast-paced environment
  • Possesses exceptional communication skills with experience leading and collaborating with diverse teams
  • Self-driven with a proactive solution-focused mindset and an ability to derive and execute scientific and operational initiatives
  • Experience with genetic variant curation, interpretation of clinical relevance, and therapy recommendations based on guidelines such as AMP/ASCO.
  • Familiarity with clinical testing regulatory requirements including FDA, CAP, and NYS.

 

 

 

#LI-SH1
#LI-Remote