出海雷达

高级转化医学科学家(女性健康)

Sr Translational Med Scientist (Women's Health)

其他限定地区(需当地身份)
公司Natera
薪资未公开
工作地点US Remote
地域资格限定地区(需当地身份)
时区要求无特别要求
用工类型未标注
发布时间15 天前
数据来源Greenhouse
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注意地域限制:该职位明确限定在 US Remote 招聘。如果你是位于中国大陆的求职者,通常需要当地工作身份才能投递,或需与雇主确认是否接受独立合同(Contractor)形式合作。

职位概述
我们正在寻找一位临床转化科学家(TMED),对女性健康研究充满热情,并在医学遗传学和基因组学方面具有专业知识。该职位将与跨职能团队和外部合作伙伴紧密合作,利用其在临床研究和基因组学方面的专业知识,推动可操作的见解,并指导研究项目和科学出版物的开发。该职位提供了一个独特的机会,在快速发展的环境中结合生物统计学、临床研究和转化医学。

主要职责
1. 深入了解女性健康临床和商业数据
• 作为所有与女性健康产品和临床试验相关的内部临床和商业数据的主要联系人。
• 建立结构和流程以整理和管理数据集。
• 跟踪数据类型和来源(例如电子健康记录、真实世界数据、商业实验室数据、临床试验),以优化用于医学教育、出版物和产品开发的使用。
• 强化数据治理流程,确保数据准确性、质量和监管合规性。

2. 数据分析与研究规划
• 设计并执行基因组学和临床分析,探索女性健康领域的生物学、科学和临床问题。
• 支持研究计划,与临床运营团队合作,确保适当的数据采集、研究设计和方案开发。
• 监控研究领域,评估新兴技术和竞争趋势。

3. 与跨职能团队协作
• 与数据科学家和生物统计团队一起对女性健康数据集进行深入分析。
• 与内部团队(如临床运营、研发、生物统计、产品管理、外部站点研究人员和关键意见领袖)合作,确保研究和试验的高效执行。

4. 出版与沟通
• 与相关利益相关者和关键意见领袖合作,准备用于同行评审出版物和学术会议的摘要、海报和论文。
• 向内部和外部受众(包括临床医生、学术合作伙伴和跨职能利益相关者)展示研究成果。
• 将技术发现转化为清晰、可操作的见解,供组织内决策者参考。

5. 合规与隐私
• 处理PHI(受保护健康信息)

查看英文原文

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.

The pay range is listed and actual compensation packages are based on a wide array of factors unique to each candidate, including but not limited to skill set, years & depth of experience, certifications and specific office location. This may differ in other locations due to cost of labor considerations.
Remote USA
$106,200—$132,700 USD

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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