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.
Lead the statistical design and analytical planning for oncology clinical utility studies with innovative methodologies.
Author and review high-quality statistical deliverables including SAPs and reports for cross-functional collaborators.
Mentor early career statisticians and support continuous improvement of departmental processes and tools.
Natera is a global leader in cell-free DNA testing, dedicated to oncology, women's health, and organ health. The team consists of highly dedicated professionals from world-class institutions, working in a fast-paced environment.
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.
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 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.
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.
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.
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.
Lead the identification, development, and application of innovative statistical methodologies for clinical development programs.
Provide expert statistical consultation and shape statistical strategies for clinical trial design and analysis.
Mentor statisticians and build a statistical innovation team to foster methodological excellence.
Alnylam is the leader in RNAi therapeutics, a revolutionary approach with the potential to transform the lives of people with rare and common diseases. The company is a globally recognized top employer with an authentic, inclusive culture and a deep pipeline, late-stage programs, and a bold vision.
Oversee global clinical trial execution, including site selection, activation, enrollment, and closeout, while ensuring compliance with GCP and regulatory requirements.
Partner with CROs to drive robust trial management, data monitoring, and patient enrollment strategies, and review study-related plans and documents.
Mentor and guide clinical operations team members, track performance metrics, and ensure inspection readiness across all study phases.
Summit Therapeutics is a biopharmaceutical oncology company focused on improving quality of life and resolving unmet medical needs through innovative clinical studies. With multiple global Phase 3 trials and offices across the US, UK, and Ireland, the company is committed to a collaborative, people-driven culture.
Monitor clinical trial sites to ensure compliance with protocols, SOPs, and regulatory requirements.
Review electronic medical records and source documentation for accuracy and data integrity.
Support site staff and contribute to development of trial materials, SOPs, and training guides.
Orca Bio is a commercial-stage biotechnology company developing next-generation cell therapies to improve transplant outcomes for blood cancer patients. The company maintains a start-up culture with an entrepreneurial spirit and emphasis on camaraderie.