Assistant Director of Clinical Science Oncology
at Tempus
Remote, Oregon, USA -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 30 Nov, 2024 | Not Specified | 02 Sep, 2024 | N/A | Cap,Regulatory Requirements,Human Genetics,Genomics,Communication Skills,Molecular Genetics,High Growth | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
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.
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.
Responsibilities:
- 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.
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
Remote, USA