Design and review statistical methodology for clinical trial protocols and analysis plans.
Lead execution of statistical analyses for regulatory submissions and exploratory studies.
Effectively convey complex statistical concepts to cross-functional teams and stakeholders.
Natera is a global leader in cell-free DNA testing for oncology, women's health, and organ health. The team consists of highly dedicated professionals from world-class institutions who care deeply about their work and each other.
Develop and quality-control SDTM datasets supporting clinical research and regulatory submissions.
Program complex SDTM datasets and trial design domains using SAS.
Collaborate with sponsors, data operations, and cross-functional teams to ensure timely project delivery.
This partner company is a clinical research organization that develops SDTM datasets for regulatory submissions. The environment is collaborative, fast-paced, and focused on quality and operational excellence.
Provide high-level consulting services for statistical analysis, reporting, and programming in clinical trials.
Develop and validate statistical analysis plans, randomization schedules, and clinical trial reports.
Mentor statistical programmers and ensure compliance with regulatory guidelines like ICH, GCP, and 21 CFR Part 11.
eClinical Solutions helps life sciences organizations accelerate clinical development initiatives with expert data services and the elluminate Clinical Data Cloud. It is a fast-growing company that has won the 2025 Top Workplaces USA Award for Remote Work and emphasizes an inclusive culture and work-life balance.
Lead statistical activities for clinical trials, primarily in Oncology, and act as the lead statistician overseeing strategy and deliverables.
Author key documents including Statistical Analysis Plans (SAPs), Analysis Database Specifications, and statistical sections of clinical study reports.
Collaborate with cross-functional teams, communicate results to stakeholders, and ensure regulatory compliance with FDA, ICH, and GCP standards.
ClinChoice is a global full-service CRO specializing in clinical development for pharmaceutical, biotechnology, medical device, and consumer health companies. With over 28 years of experience and 4,000+ professionals across 20+ countries, we foster a quality-driven, one-team culture with below-average turnover and a focus on continuous training.
Lead protocol development including study design and statistical analysis plans for clinical trials.
Provide statistical oversight, mentoring, and training to ensure high-quality project delivery.
Manage statistical activities across projects, ensuring accuracy and consistency with regulatory standards.
ClinChoice is a global full-service CRO specializing in clinical development for pharma, biotech, and medical device companies. With over 4,000 professionals across 20+ countries, they foster a quality-driven, one-team culture and emphasize diversity and low turnover.
Independently perform statistical analyses for clinical studies and research initiatives.
Develop statistical analysis plans, including sample size and power calculations.
Collaborate with cross-functional teams to ensure statistical rigor and appropriate interpretation of results.
Karius is a life science, venture-backed clinical metagenomics company focused on elevating patient care through microbial insights. The company delivers unprecedented diagnostic insight detecting microbial cell-free DNA to assist physicians in making rapid treatment decisions.
Set the statistical vision and direction for clinical studies spanning early feasibility through post-market evidence generation.
Manage a portfolio of 10+ projects, represent Biostatistics with regulatory agencies, and lead external scientific engagements.
Drive process improvement, mentorship, and AI-enabled productivity across the biostatistics team.
We are a global leader in robotic-assisted surgery and minimally invasive care, with technologies like the da Vinci surgical system. We are a team of engineers, clinicians, and innovators united by one purpose: to make surgery smarter, safer, and more human.
Develop, validate, and maintain SAS programs for clinical study data analysis and reporting.
Create datasets, tables, listings, and figures according to study requirements and CDISC standards.
Collaborate with Biostatistics, Data Management, and Clinical teams to ensure quality and timelines.
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. With over 28 years of experience and 4,000+ professionals across more than 20 countries, we foster a supportive culture with below-industry-average turnover.
Independently lead statistical design and analysis for preclinical studies, including dose-response modeling and aging biomarker studies.
Build and apply population PK/PD models to support internal dose-justification and formulation decisions.
Conduct exploratory analyses to support endpoint development and target/pathway discovery.
Loyal is a clinical-stage veterinary medicine company developing longevity drugs for dogs. Loyal is a well-funded startup with teams of scientists, veterinarians, engineers, operators, and creatives.
Provide expert technical support and leadership in clinical trial reporting using advanced SAS features.
Perform quality control checks and ensure accuracy and consistency of SAS code and output.
Collaborate with cross-functional teams to support electronic submissions and compliance with regulatory standards.
Vertex is a global biotechnology company that invests in scientific innovation to create transformative medicines for people with serious diseases. With over 30 years of history, the company is consistently recognized as one of the industry's top places to work, including 14 consecutive years on Science magazine's Top Employers list and one of Fortune’s 100 Best Companies to Work For.
Draft and contribute to Statistical Analysis Plans (SAP) and methodological documentation for RWE studies.
Program analyses in R and Python, with basic SQL/PostgreSQL, and set up data quality checks.
Produce decision-ready deliverables (tables, figures, reports) and communicate insights to non-statisticians.
Resilience Care is a French remote patient monitoring company founded in 2021, providing RPM solutions in oncology, gastroenterology, and psychiatry by combining ePRO collection with AI. They serve 35,000 patients across 200+ healthcare institutions and support around twenty clinical studies, fostering a culture of data-driven care and therapeutic innovation.
Lead and support statistical programming deliverables for oncology clinical studies.
Ensure high-quality programming with CDISC standards and regulatory compliance.
Collaborate with cross-functional teams including statisticians, data managers, and study leaders.
ClinChoice is a global full-service CRO specializing in clinical development for pharmaceutical, biotechnology, medical device, and consumer health companies. They have over 28 years of experience and over 4,000 professionals in more than 20 countries, with a culture focused on quality, professional development, and supportive collaboration.
Provide statistical leadership and consultation for an international real-world clinico-genomic data consortium.
Develop statistical analysis plans, perform statistical programming in R, and design observational studies.
Collaborate with investigators, pharmaceutical clients, and academic institutions to translate research questions into rigorous analyses.
The American Association for Cancer Research (AACR) is the first and largest organization in the world dedicated to advancing cancer research, with over 61,000 members in 143 countries. It fosters collaboration among scientists, physicians, and patient advocates to prevent and cure cancer through publications, conferences, and advocacy.
Manage a team of statistical programmers supporting clinical research and ensuring quality, integrity, and timely delivery of programming deliverables.
Provide statistical programming support, oversee development of code for Tables, Listings, and Figures, and ensure compliance with quality processes.
Lead resource planning, manage CROs, and contribute to process improvements and innovation in statistical programming standards.
Penumbra is a global healthcare company focused on innovative therapies, designing and marketing novel products for challenging medical conditions. It sells primarily through a direct sales organization in the US, Europe, Canada, and Australia.
Develops and analyzes research data using statistical methods, assisting researchers with study protocols and computer analyses.
Manages computer systems, writes programs, and trains others in their use, providing statistical expertise in study design and data analysis.
Consults with investigators to determine research questions, performs appropriate statistical analyses, and documents methods and results in reports.
Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate today and prepare leaders for the future. It is a large institution with a diverse academic community, committed to equal opportunity and affirmative action.