Provide statistical programming support for clinical trials and produce analyses, including generating and validating SDTM/ADaM datasets, tables, listings, and figures.
Work under the direction of senior programmers to review Statistical Analysis Plans and apply appropriate statistical methods.
Assist in developing SAS macros, participate in validation and quality control, and collaborate with cross-functional teams.
Support development and validation of datasets, tables, figures, and listings for clinical trials using SAS and/or R.
Assist with CDISC-compliant SDTM and ADaM datasets, Define-XML, and electronic submission deliverables.
Perform programming validation, quality checks, and collaborate with cross-functional teams to meet project timelines.
ClinChoice is a global full-service CRO supporting 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 quality-driven one-team culture and continuous employee training.
Develop and validate SAS and R programs to produce CDISC-compliant datasets and TLFs for clinical studies.
Serve as lead programmer on late-phase studies and regulatory submissions, ensuring high-quality, audit-ready deliverables.
Collaborate with cross-functional teams and mentor junior programmers to support statistical programming standards.
Pulmovant is a clinical-stage biotechnology company developing treatments for pulmonary diseases, including its lead candidate mosliciguat for PH-ILD. As part of the Roivant family, it emphasizes collaboration and innovation in advancing its pipeline.
Lead biostatistics activities across clinical studies, ensuring high-quality analyses and clear communication.
Provide statistical expertise for oncology trials, from protocol development to regulatory submissions.
Oversee statistical programming and deliverables, ensuring quality, integrity, and compliance.
Jobgether is a platform that uses AI-powered matching to connect candidates with hiring companies, focusing on objective and fair application reviews. The company is dynamic and emphasizes a streamlined hiring process, with a data-driven approach and a commitment to innovation.
Provide statistical expertise and hands-on support for Phase III oncology clinical trials, including study design and analysis.
Author and review TFL and ADaM specifications, collaborating closely with Statistical Programming.
Manage deliverables across multiple concurrent clinical studies, ensuring timelines and quality expectations are met.
ClinChoice is a global full-service CRO supporting pharmaceutical, biotechnology, medical device, and consumer health companies in clinical development. With over 4,000 professionals in more than 20 countries, they emphasize a quality-driven 'one-team' culture and below-industry-average turnover.
Lead statistician for clinical studies, responsible for study design, analysis, and documentation.
Collaborate with cross-functional teams and manage external vendor work.
Provide statistical expertise for regulatory submissions and act as subject matter expert.
Jazz Pharmaceuticals is a global biopharma company developing life-changing medicines for serious diseases, focusing on oncology and neuroscience. With employees in multiple countries, it fosters a patient-focused, science-driven culture.
Own statistical strategy across the portfolio while staying hands-on as lead statistician on live programmes.
Serve as primary statistical interface with regulators and assess in-licensing assets' statistical rigour during due diligence.
Build and lead the biostatistics, statistical programming, and medical writing functions as the team grows.
Lindus Therapeutics is building the next generation of biopharma by in-licensing clinical-stage assets and developing them through Lindus Health's technology-first clinical trial infrastructure. It is a new, small team with a proven foundation of 40+ completed trials.