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.
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.
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.
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.
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.
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.
Lead technical sales engagements with healthcare and life sciences clients, gathering requirements and demonstrating SLC capabilities.
Conduct proof-of-concept activities and provide architectural guidance for deploying SLC in existing IT ecosystems.
Act as a subject matter expert in SAS language and statistical programming, authoring industry-specific presentations and workshops.
Siemens Software is a leading industrial software company that builds technology to shape the real world. With 30,000 employees across more than 200 countries, we foster a culture of trust, autonomy, and inclusion.
Provide statistical expertise across clinical development programs, authoring SAPs and overseeing ADaM/TFL deliverables.
Contribute to innovative trial designs, regulatory submissions, and cross-functional collaboration with clinical teams.
Ensure high-quality statistical analyses and compliance with regulatory requirements in a remote/hybrid setting.
The partner company specializes in global clinical development, supporting registration-directed clinical trials across therapeutic areas. It fosters a collaborative, results-oriented culture with a focus on innovation, professional growth, and high-quality deliverables.
Lead the development and optimization of clinical data systems across global trials.
Drive data standardization and build scalable validation frameworks to ensure data integrity.
Act as a strategic liaison between clinical, biostatistics, and regulatory teams to translate requirements into technical solutions.
Precision Medicine Group is a global life sciences company focused on precision medicine and clinical research solutions. The company fosters a collaborative and compliance-oriented culture with a diverse team of professionals.
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.
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.
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.
Act as a trusted advisor to customers and clinical sites, ensuring trial designs meet goals and providing training.
Lead database development activities, configure forms and rules in Vault CDMS, and build custom SQL listings.
Support requirements gathering, user acceptance testing, and risk management to keep projects compliant.
Veeva Systems is a mission-driven pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies, it surpassed $3B in revenue and is a public benefit corporation committed to balancing stakeholder interests.