Senior Translational Med Scientist, Women's Health

This is a fully remote position, open to applicants in United States.

📋 Description

• Act as the main liaison for internal clinical and commercial data concerning women’s health products and clinical trials.

• Establish frameworks and processes for curating and overseeing datasets.

• Monitor data types and sources, including EHR, real-world data, commercial lab data, and clinical trials.

• Strengthen data governance protocols to guarantee data accuracy, quality, and adherence to regulatory standards.

• Develop and implement genomic and clinical analyses that address biological, scientific, and clinical inquiries in women’s health.

• Assist in study planning with clinical operations, covering data capture, study design, and protocol creation.

• Keep abreast of the research landscape and assess emerging technologies and competitive dynamics.

• Collaborate with data scientists and biostatisticians on analyses of women’s health data sets.

• Partner with clinical operations, research and development, biostatistics, product management, external site investigators, and key opinion leaders.

• Prepare abstracts, posters, and manuscripts for submission to peer-reviewed journals and academic conferences.

• Present findings to clinicians, academic partners, and cross-functional stakeholders.

• Convert technical results into actionable insights for organizational leaders.

• Manage protected health information while ensuring compliance with HIPAA and Natera policies.

⛳️ Requirements

• Ph.D. in Clinical Science, Molecular Biology, Genomics, Bioinformatics, Genetics, or related fields.

• Strong scientific background in molecular genomics, ideally in women's health.

• Proven experience with genetic data and nomenclature.

• Familiarity with real-world clinical data, such as EMR and LIMS, along with knowledge of clinical parameters and variable definitions.

• Demonstrated expertise in project management.

• Experience collaborating with external partners and key opinion leaders.

• Proficiency in data mining, data curation, statistical analysis tools, and methodologies.

• Expertise in R programming, including ggplot2, data.table, and Bioconductor.

• Knowledge of querying relational databases using SQL.

• Experience in predictive modeling, epidemiological methods, and clinical observational and retrospective study designs.

• Familiarity with clinical trial processes, IRB requirements, and relevant FDA or equivalent regulations.

• Ability to manage multiple projects, prioritize responsibilities, and meet deadlines.

• Exceptional verbal and written communication abilities.

• Strong interpersonal skills with experience leading or working collaboratively in cross-functional teams.

• Must manage PHI in accordance with HIPAA regulations and Natera policies.

• Must fulfill current organizational training requirements and successfully complete a post-offer criminal background check.

🏝️ Benefits

• Comprehensive medical, dental, vision, life, and disability plans for eligible employees and their dependents.

• Complimentary testing for Natera employees and their immediate families.

• Fertility care benefits.

• Leave for pregnancy and baby bonding.

• 401(k) benefits.

• Commuter benefits.

• Employee referral program.

• Equal Opportunity Employer fostering a diverse and inclusive workplace.