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 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.
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 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.
Lead data management activities for clinical and epidemiologic research studies from start-up through closeout.
Perform advanced SAS programming to clean, validate, and manage complex research datasets.
Design and maintain study databases, validation rules, and data quality procedures.
DLH delivers improved health and national security readiness solutions for federal programs through science research and development, systems engineering, and digital transformation. The company employs experts in public health and health operations and is committed to innovation and improving lives.
Develop and maintain clinical data listings, reports, and programming solutions to support data review and safety monitoring.
Analyze requirements from Data Management and Risk-Based Study Management teams and create efficient programming solutions.
Ensure all activities comply with regulatory requirements, industry guidelines, and internal procedures.
A partner company in the clinical research industry supports global clinical research programs through data analysis and programming. The company offers a fully remote, collaborative environment with a focus on continuous learning and improvement.
Provide statistical oversight and lead complex programs such as NDA/BLA/MAA submissions.
Consult with clients on clinical trial study design and regulatory strategy.
Author statistical analysis plans and review statistical output for accuracy.
Precision Medicine Group provides statistical leadership and support for clinical development, consulting with clients on trial design and regulatory strategy. The company is a global organization that values collaboration, service, and accountability, fostering a culture of mentoring and innovation.
Leads a global team of Statistical Programmers, overseeing SDTM, ADaM, and TLF deliverables.
Ensures quality, budget, and timeline adherence while mentoring team members.
Contributes to process improvements and strategic initiatives to enhance operational efficiency.
Ergomed is a specialist clinical research organization focused on rare disease and oncology clinical trials. They have built a collaborative, international team across multiple continents, valuing teamwork, flexibility, and work-life balance.
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.
Manage all programming aspects of clinical databases from study start to post-lock, ensuring compliance with regulatory guidelines.
Lead operational study teams and provide technical training to end users and junior staff.
Communicate project status to internal teams and clients, and perform project forecasting and budget management.
Precision for Medicine is a life sciences company that provides clinical research services, including database programming and data management. The company is growing and seeks a Principal Database Programmer to join its European team, fostering a collaborative and dynamic work environment.
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.
Lead the development and execution of statistical analysis plans for large-scale real-world evidence studies.
Work directly with cross-functional teams and senior stakeholders to design data-driven solutions for a high-profile sponsor.
Oversee and mentor junior analysts, driving best practices and innovative analytics workflows.
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 4,000 professionals in more than 20 countries, the company emphasizes a supportive culture, continuous training, and below-industry-average turnover rates.
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.
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.