Sr. Translational Medical Scientist at Natera

San Carlos, California, United States

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Not SpecifiedCompensation

Senior (5 to 8 years), Expert & Leadership (9+ years)Experience Level

Full TimeJob Type

UnknownVisa

Biotechnology, Healthcare, OncologyIndustries

Requirements

Ph.D. in Molecular Biology, Genomics, Cancer Biology, Genetics, Molecular Biology, or equivalent
Minimum of 5+ years of relevant experience
Deep scientific understanding or education background in oncology
Specific experience with circulating nucleic acids and early cancer detection methods such as methylation, SNV/indel panels, and fragmentation preferred
Knowledgeable and experienced in the use and optimization of novel technologies and awareness of the competitive landscape
Working knowledge of basic bioinformatics and genomics sequencing analysis techniques
Knowledge of data mining and statistical analysis tools such as R, SQL, or Stata is a plus
Excellent verbal and written communication skills
Strong organizational and interpersonal skills
Complete training relating to HIPAA/PHI privacy, General Policies and Procedure Compliance training, and security training within first 30 days of hire
Maintain current status on Natera training requirements

Responsibilities

Work with R&D, clinicians, product managers, and KOLs to identify specimen biobanks to support early cancer detection assay development
Apply knowledge of genomics, molecular biology, and cancer biology to evaluate commercial and research opportunities in early cancer detection
Collaborate with molecular biologists, computational biologists, and statisticians to build research strategies that solve challenging problems
Perform genomic analysis to explore biological, scientific, and clinical questions in oncology and translate results to impact patient care
Lead internal efforts on oncology knowledge management and curation
Collaborate with external partners, including academic KOLs, biotechnology companies, and pharmaceutical companies
Communicate results and findings of analyses to academic researchers and collaborate to publish findings in high impact journals
Oversee and train scientists and research associates
Support regulatory affairs team by assisting with responses to regulatory agency questions (CLIA, CAP, FDA) regarding product design and validations
Performs other duties as assigned
Partners with clinicians, product managers, and key opinion leaders (KOLs) in applying genomic data to advance healthcare
Participate in ongoing translational initiatives to optimize ctDNA testing, inform clinical decisions, and improve outcomes in patients with solid and hematological malignancies
Integrate genomic and clinical data across multiple high-impact projects in a fast-paced environment
Build and expand a team to meet evolving company needs in early cancer detection and other translational objectives
Works with PHI on a regular basis both in paper and electronic form and have access to various technologies to access PHI

Skills

Key technologies and capabilities for this role

genomicsmolecular biologycancer biologyctDNA testinggenomic analysisoncologytranslational medicinebiobanksregulatory affairsCLIA

Questions & Answers

Common questions about this position

What qualifications are required for the Sr. Translational Medical Scientist role?

A Ph.D. in Molecular Biology, Genomics, Cancer Biology, Genetics, or equivalent is required, along with a minimum of 5+ years of relevant experience.

What key skills and experience are needed for this position?

Candidates need a deep scientific understanding in oncology, specific experience with circulating nucleic acids, and early cancer detection methods such as methylation, SNV/indel panels, and fragmentation.

What is the salary or compensation for this role?

This information is not specified in the job description.

Is this position remote or does it require office work?

This information is not specified in the job description.

What does the team structure look like for this role?

The role involves leading and expanding a team, including overseeing and training scientists and research associates, in a cross-functional environment with R&D, clinicians, product managers, and external partners.

Natera

Genetic testing and diagnostics solutions provider

About Natera

Natera focuses on genetic testing and diagnostics, providing advanced solutions for cancer patients, transplant patients, and individuals assessing hereditary health risks. Their main technology is cell-free DNA (cfDNA) testing, which analyzes DNA fragments in the blood to detect minimal traces of cancer and assess organ health. Natera stands out by offering specialized tests like the Signatera ctDNA test and Panorama NIPT, along with genetic counseling services. The company's goal is to improve patient care and health outcomes through accurate genetic testing.

Austin, TexasHeadquarters

2004Year Founded

$149.9MTotal Funding

IPOCompany Stage

Biotechnology, HealthcareIndustries

1,001-5,000Employees

Benefits

Flexible medical plans

Investment options

Time off

Workplace perks

Risks

Hindenburg report accuses Natera of deceptive sales practices, risking legal challenges.

New Prospera Heart features may face slow adoption by healthcare providers.

Fetal RhD NIPT demand may drop post-RhIg shortage, affecting future sales.

Differentiation

Natera's Signatera test offers personalized ctDNA analysis for cancer patients.

Prospera Heart test uses unique Donor Quantity Score for transplant rejection detection.

Panorama NIPT test is a leader in non-invasive prenatal testing with 2 million tests.

Upsides

Increased adoption of liquid biopsy techniques boosts demand for Natera's cfDNA tests.

AI integration enhances accuracy and speed of Natera's cfDNA analysis.

Growing personalized medicine trend aligns with Natera's customized genetic tests.

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