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.
Design, develop, and validate CDISC-compliant SDTM and ADaM datasets for clinical trials.
Support regulatory submissions including ISS, ISE, and create Tables, Listings, and Figures.
Collaborate with cross-functional teams to deliver accurate statistical outputs for evidence-based healthcare.
The partner company is a clinical research organization that supports impactful clinical programs through statistical programming. It offers a collaborative culture and a flexible remote work environment.
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.
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.
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.
Develop, validate, and maintain SAS and/or R programs for SDTM, ADaM datasets, and TLFs per CDISC standards.
Support statistical analyses for regulatory submissions, safety reports, and clinical study reports in a GxP-compliant environment.
Collaborate with cross-functional teams to define analysis specifications and perform quality control on statistical outputs.
Iovance Biotherapeutics is a global leader in innovating, developing, and delivering tumor infiltrating lymphocyte (TIL) therapy for cancer. The company is a fast-paced biotech with a collaborative culture, committed to continuous innovation in cell therapy.
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.
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.
Apply advanced statistical expertise to support impactful clinical research and data-driven decision-making.
Lead statistical analysis activities for clinical trial programs, ensuring data accuracy, scientific rigor, and clear reporting.
Collaborate with multidisciplinary teams to interpret results, support decision-making, and deliver high-quality statistical outputs.
Jobgether is an AI-powered job matching platform connecting candidates with hiring companies. It uses automated screening to shortlist top-fitting candidates for each role.
Lead the development, testing, and support of clinical databases from startup through post-lock.
Partner with Data Management, Project Management, EDC vendors, and clients to guide database design and programming.
Mentor junior programmers, train end users, and shape the new regional team's growth and processes.
Precision Medicine Group is a specialized life sciences company that accelerates the development and commercialization of precision medicines. The company is expanding across LATAM and values collaboration, technical leadership, and innovation.
Lead the full scope of Biostatistics activities for assigned clinical programs, including study design, analysis, and regulatory submissions.
Collaborate cross-functionally with Clinical, Medical, and Regulatory teams to ensure quality and timely delivery of statistical outputs.
Oversee CROs and internal teams, supervise statistical programming, and drive continuous improvement in biostatistics processes.
Mineralys Therapeutics is a clinical-stage biopharmaceutical company focused on developing medicines to target hypertension and related comorbidities. The company is headquartered in Radnor, Pennsylvania and operates as a fully remote organization.
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.