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Sr Translational Med Scientist (Women's Health)

Role overview

Qualifications

  • Ph.D. in Clinical Science, Molecular Biology, Genomics, Bioinformatics, Genetics, or related disciplines.
  • Strong scientific foundation in molecular genomics perspectives, preferably in the women’s health space.
  • Demonstrated experience working with genetic data and nomenclature.
  • Demonstrated project management experience.

Responsibilities

  • Serve as the primary point of contact for all internal clinical and commercial data relating women’s health products and clinical trials.
  • Design and execute genomic and clinical analyses to explore biological, scientific, and clinical questions in women’s health.
  • Collaborate with cross-functional teams to ensure efficient execution of studies and trials.
  • Collaborate with relevant stakeholders on the preparation of abstracts, posters, and manuscripts for peer-reviewed publications.

Key facts

  • Remote from: United States
  • Full time
  • Senior (5-10 years)
  • Physicist
  • English

Hard skills

Other skills

  • Communication
  • Collaboration
  • Problem Solving
  • Adaptability
  • Teamwork

About the company

Natera logo

Natera

Genomics & Precision Medicine

Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives. Where some set out to build a test, we set out to achieve a mission: change the management of disease worldwide by using DNA testing to proactively inform treatment.  Through a cfDNA technology platform approach, we've pioneered noninvasive testing in unlimited applications—each with their own potential to revolutionize care for patients. #TeamNatera includes clinicians, scientists, biostatisticians, researchers, and laboratory professionals from around the world. Our diverse teams blend a passion for patients with deep clinical, scientific, and technological roots. Natera’s tests are validated by more than 100 peer-reviewed publications that demonstrate high accuracy. Interested in joining us on our mission to change the management of disease worldwide? Visit https://www.natera.com/careers-at-natera to learn how you can become a part of our talented team. Natera operates ISO 13485-certified and CAP-accredited laboratories certified under the Clinical Laboratory Improvement Amendments (CLIA) in Austin, Texas and San Carlos, California. Please be advised that Natera will reach out to candidates with an @natera.com email domain ONLY. Email communications from all other domain names are not from Natera or its employees and are fraudulent. Natera does not request interviews via text messages and does not ask for personal information until a candidate has engaged with the company and has spoken to a recruiter and the hiring team. Natera takes cyber crimes seriously, and will collaborate with law enforcement authorities to prosecute any related cyber crimes. https://www.natera.com/privacy/

Company details

Company typeLarge
IndustryGenomics & Precision Medicine
Company size1001 - 5000

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Job description

Position Summary
We are seeking a Clinical-Translational Scientist, (TMED) with a passion for Women’s Health research and expertise in medical genetics and genomics. This individual will collaborate closely with cross-functional teams and external partners, using their expertise in clinical research and genomics to drive actionable insights, and guide the development of research projects and scientific publications. This position offers a unique opportunity to blend biostatistics, clinical research, and translational medicine in a rapidly evolving environment.

Key Responsibilities
1.    In Depth Knowledge of Internal Women’s Health Clinical and Commercial Data
•    Serve as the primary point of contact for all internal clinical and commercial data relating women’s health products and clinical trials.
•    Implement structures and processes for curating and managing datasets
•    Track the types and sources of data (e.g., EHR, real-world data, commercial laboratory data, clinical trials) to optimize use for medical education, publications, and product development.
•    Reinforce processes for data governance, ensuring data accuracy, quality, and regulatory compliance.
2.    Data Analysis & Study Planning
•    Design and execute genomic and clinical analyses to explore biological, scientific, and clinical questions in women’s health.
•    Support the planning of studies collaborating with clinical operations to ensure appropriate data capture, study design, and protocol development.
•    Monitor the research landscape and evaluate emerging technologies and competitive trends
3.    Collaborate with Cross-Functional Teams 
Work side-by-side with data scientists and biostatistics team to perform robust analyses on women’s health datasets.
•    Partner with internal teams such as clinical operations, research & development, biostatistics, product management, external site investigators, and key opinion leaders to ensure efficient execution of studies and trials.
4.    Publication & Communication
•    Collaborate with relevant stakeholders and key opinion leaders on the preparation of abstracts, posters, and manuscripts for peer-reviewed publications and academic conferences.
•    Present results to internal and external audiences, including clinicians, academic partners, and cross-functional stakeholders.
•    Translate technical findings into clear, actionable insights for decision-makers across the organization.
5.    Compliance & Privacy
•    Handle PHI (Protected Health Information) and ensure compliance with HIPAA regulations and Natera policies.
•    Maintain a current status on organizational training requirements and pass a post- offer criminal background check.

Qualifications
•    Ph.D. in Clinical Science, Molecular Biology, Genomics, Bioinformatics, Genetics, or related disciplines.
•    Strong scientific foundation in molecular genomics perspectives, preferably in the women’s health space.
•    Demonstrated experience working with genetic data and nomenclature. Variant curation experience and knowledge a plus. 
•    Experience working with real-life clinical data (e.g., EMR, LIMS, etc.) and knowledge of clinical parameters and variable definitions.
•    Demonstrated project management experience is a must 
•    Demonstrated experience working with external collaborators/KOLs a must. 
•    Proficiency in data mining, data curation, statistical analysis tools, and methodologies.
•    Expertise in R programming, including packages such as ggplot2, data.table, and Bioconductor.
•    Familiarity with querying relational databases using SQL.
•    Demonstrated experience with predictive modeling, epidemiological methodology, clinical observational and retrospective study design. Familiarity with machine learning algorithms, computational modeling, or other advanced data science methodologies is beneficial.

Knowledge, Skills, and Abilities
•    Clinical Research & Regulations: Working knowledge of clinical trial processes, IRB requirements, and relevant FDA or equivalent regulations.
•    Project Management: Adept at juggling multiple projects, prioritizing tasks, and meeting deadlines in a fast-paced environment with shifting priorities. Proven success in managing collaborative and individual projects.
•    Communication & Collaboration: Excellent verbal and written communication skills; ability to convey complex scientific concepts to both technical and non-technical stakeholders.
•    Adaptability & Problem-Solving: Solutions-oriented approach; identifies potential challenges or risks and proposes effective resolutions. Experience working in dynamic departments where priorities change quickly.
•    Team Player: Strong interpersonal skills; experience leading or collaborating with cross-functional teams, including data science, clinical operations, and external stakeholders.

Preferred Qualifications
•    Experience managing clinical trials including contracting, budgeting, and protocol design experience.
•    Experience in publishing research in high-impact journals.
•    Knowledge of emerging trends and society guidelines in women’s health. 
•    Provide coding and statistical support using Python and R for data exploration, modeling, and interpretation.

OUR OPPORTUNITY

Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives.

The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you’ll work hard and grow quickly. Working alongside the elite of the industry, you’ll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.

WHAT WE OFFER

Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more. We also offer a generous employee referral program!

For more information, visit www.natera.com.

Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide.

All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws.

If you are based in California, we encourage you to read this important information for California residents. 

Link: https://www.natera.com/notice-of-data-collection-california-residents/

Please be advised that Natera will reach out to candidates with a @natera.com email domain ONLY. Email communications from all other domain names are not from Natera or its employees and are fraudulent. Natera does not request interviews via text messages and does not ask for personal information until a candidate has engaged with the company and has spoken to a recruiter and the hiring team. Natera takes cyber crimes seriously, and will collaborate with law enforcement authorities to prosecute any related cyber crimes.

For more information:
- BBB announcement on job scams 
- FBI Cyber Crime resource page 

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Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
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