Remote Data Jobs · CDISC

Job listings

US Europe 5w PTO 16w maternity 6w paternity

  • 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.

  • 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.

  • 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.

  • 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.

  • 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.