Variant Scientist (Part-time, Remote)
at Personalis Inc
Remote, Oregon, USA -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 28 Oct, 2024 | USD 66000 Annual | 28 Jul, 2024 | 2 year(s) or above | Communication Skills,Base Pay,Critical Thinking,Medical Terminology,Disabilities,Genetic Counseling,Genetics,Clinical Documentation,Cancer Biology | 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:
At Personalis, we are transforming the active management of cancer through breakthrough personalized testing. We aim to drive a new paradigm for cancer management, guiding care from biopsy through the life of the patient. Our highly sensitive assays combine tumor-and-normal profiling with proprietary algorithms to deliver advanced insights even as cancer evolves over time. Our products are designed to detect minimal residual disease (MRD) and recurrence at the earliest timepoints, enable selection of targeted therapies based on ultra-comprehensive genomic profiling, and enhance biomarker strategy for drug development. Personalis is based in Fremont, California.
POSITION SUMMARY
We are looking for a part time variant scientist with a strong molecular genetics and genomics background, and familiarity with next-generation sequencing technologies. You will play a key role in delivering cutting-edge, production-quality genome interpretation for clinical and research products in the field of cancer diagnostics. You will work with a team of genetic counselors, variant scientists and molecular pathologists to deliver on time clinical diagnostic reports. The position can be remote anywhere in the US.
EDUCATION AND EXPERIENCE
- MS degree in Genetic Counseling, or MS/PhD degree in Human/Medical/Molecular Genetics or related field
- Exceptional Bachelor’s degree candidates with 2+ years of related experience may be considered
- Knowledge of NGS-based testing technologies and related bioinformatics workflows
- Experience with clinical documentation and medical terminology
- Understanding of cancer biology and genetics
- Ability to understand and interpret complex information in the scientific literature
- Attention to detail with excellent written and verbal communication skills
- Strong critical thinking and problem-solving skills
- Desire and ability to work independently in a demanding, high-tech environment
This is a salaried part-time job (.5 FTE) requiring approximately 20 hours a week, distributed as ~4 hours per day. The salary for this position ranges from $52,500 to $66,000 annually. Please note that this part-time role does not include health benefits, vacation time, or sick leave. However, employees will have the opportunity to participate in the 401(k) program. The base pay actually offered will take into account internal equity and also may vary depending on the candidate’s geographic region, job-related knowledge, skills, and experience among other factors. Our salaried part-time regular positions also include an annual performance-based bonus and long-term incentive units (equity) provided as part of our compensation package.
Personalis is an equal opportunity employer and is committed to the full inclusion of all individuals. As part of this commitment, Personalis will ensure that persons with disabilities are provided with reasonable accommodations. If you need an accommodation to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please let your recruiter know, if/when they contacts you.
Personalis is an Equal Opportunity Employer/Minorities/Females/Veterans/Disabilities.
LI-Remote #LI-KK1
Responsibilities:
- Analyze, interpret, and curate information for genetic and genomic variants identified on next-generation sequencing
- Perform somatic and germline variant classification according to internal SOPs and published guidelines
- Evaluate case data, create and write content for clinical diagnostic reports from tumor comprehensive genomic profiling (CGP)
- Work collaboratively, independently, and know when to ask for help
REQUIREMENT SUMMARY
Min:2.0Max:7.0 year(s)
Hospital/Health Care
Pharma / Biotech / Healthcare / Medical / R&D
Health Care
Graduate
Human/medical/molecular genetics or related field
Proficient
1
Remote, USA