Serve as study statistician or support statistician on Bronchiectasis or Hepatitis B programs, responsible for protocol development, study design, sample size calculation, randomization, and statistical analysis plans.
Provide statistical oversight to studies, assure data completeness and accuracy, and ensure validity of analysis and alternative strategies when unforeseen circumstances arise.
Demonstrate extensive understanding of statistical concepts, correct flaws in reasoning and interpretation, and ensure accuracy of statistical tables, figures, and report text.
Maintains responsibility for all assigned biostatistics duties within clinical studies, including acting as study lead for multiple or complex studies.
Reviews and develops clinical program designs, protocols, and statistical analysis plans, ensuring high-quality and valid content.
Provides mentoring to junior statisticians and represents the biostatistics function in internal and external meetings and audits.
Ergomed Group is a rapidly expanding full-service mid-sized CRO specialising in Oncology and Rare Disease. Since 1997, the company has grown organically with operations in Europe, North America and Asia, fostering a true international culture that values employee experience, well-being, and work-life balance.
Lead the design, analysis, and interpretation of clinical studies for rare disease and oncology trials.
Oversee all contracted statistical activities, including protocol development, statistical analysis plans, and data review.
Provide mentorship to junior statisticians and represent the biostatistics function in cross-functional meetings and audits.
Ergomed is a specialist clinical research organization focused on rare disease and select oncology indications. With a global team across five continents, they value teamwork, flexibility, and work-life balance.
Leads statistical activities for clinical studies in oncology.
Authors statistical sections of study protocols, analysis plans, and regulatory documents.
Collaborates with cross-functional teams and CROs to ensure high-quality deliverables.
Iovance Biotherapeutics develops tumor infiltrating lymphocyte (TIL) therapy for cancer treatment. The company is a global leader in cell therapy innovation with a focus on clinical data and regulatory submissions.
Lead product-level biostatistics tasks including regulatory interactions and filings, ensuring statistical integrity.
Contribute to study design, sample size determination, and author/review statistical analysis plans and TFL specifications.
Mentor junior team members and collaborate cross-functionally to meet product deliverables and timelines.
Ultragenyx is a biopharmaceutical company focused on developing life-changing treatments for rare diseases. The company fosters a supportive, inclusive culture emphasizing learning and growth, enabling employees to thrive professionally and personally.
Lead the biometrics team including statisticians, data managers, and statistical programmers at a program level, providing strategic input for clinical development.
Author and develop Statistical Analysis Plans (SAPs), contribute to trial designs, protocol development, and sample size calculations, and oversee vendor deliverables.
Interact with global health authorities, contribute to regulatory submissions, and coordinate statistical analyses for safety updates and ad hoc requests.
Spyre Therapeutics is a clinical-stage biotechnology company developing next-generation long-acting antibodies to redefine the standard of care for inflammatory bowel disease and rheumatic diseases. As a growing company, they offer a fast-paced, dynamic environment where you help shape the culture and contribute broadly to meaningful medicines.
Develop, validate, and maintain SDTM and ADaM datasets using R following CDISC standards.
Support TLF generation in R or SAS as needed for clinical trial deliverables.
Collaborate with biostatistics and clinical data teams to ensure regulatory compliance and quality.
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, and medical device companies. They have over 4,000 professionals in more than 20 countries and emphasize a culture of low turnover, diversity, and inclusivity.
Participate in CRF design, database review, and data validation procedures to ensure data integrity.
Produce data listings, summary tables, and graphics for interim and final analyses of clinical trials.
Collaborate with Biometrics functions and coordinate data transfer standards with CROs and vendors.
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 across the Americas, Europe, and Asia-Pacific, they maintain a supportive culture focused on quality, professional development, and low turnover.
Support clinical data intake, cleaning, and preparation of analysis-ready datasets for model development and clinical validation.
Conduct exploratory and statistical analyses for retrospective and prospective oncology studies.
Generate tables, figures, and summary outputs for internal review, publications, and regulatory submissions.
Artera is an AI startup developing medical artificial intelligence tests to personalize therapy for cancer patients. It offers a 3-month graduate program with structured mentorship for statisticians to gain hands-on experience in biostatistics and AI healthcare.
Provide statistical leadership across clinical research projects, ensuring high-quality methodologies and analyses.
Collaborate with cross-functional teams to support innovative study designs and advanced statistical modeling.
Author and review Statistical Analysis Plans (SAPs), tables, listings, and figures for regulatory submissions.
The partner company provides advanced statistical expertise and scientific leadership within a collaborative biometrics and data science environment, supporting complex clinical research projects across multiple therapeutic areas. The company fosters a collaborative and supportive culture focused on technical excellence and innovation, with a team of experienced professionals.
Act as a domain authority establishing benchmarks for AI-driven statistical results.
Provide knowledge sharing about day-to-day workflows and regulatory submissions.
Identify and correct discrepancies in data quality and generate reference artifacts.
Edison Scientific builds and commercializes AI agents for science. We are assembling a team of top researchers and engineers across AI and biology to build an AI scientist.