Compile, format, quality-check, and redact clinical and regulatory documents for global submissions and disclosure, ensuring accurate, consistent, submission-ready deliverables that meet sponsor and regulatory requirements.
Quanticate jobs
Global biometrics CRO specializing in statistical analysis, data capture, and clinical trial reporting.
6 open roles at Quanticate
Leads and delivers regulatory and scientific medical writing projects, producing accurate, compliant clinical documents while coordinating reviews, partnering with clients, and mentoring colleagues.
Leads the proposals function, developing and quality-checking clinical bids, budgets, and pricing strategies while improving proposal processes and supporting commercial growth across teams.
Senior clinical programmer who develops and validates SAS datasets and outputs for clinical trials, contributes to study-level programming, and mentors junior colleagues to support high-quality research and regulatory decisions.
Program SAS and SQL outputs for Real World Evidence projects, working with large longitudinal healthcare datasets to support outcomes research, maintain quality, and improve clinical programming practices.
Spontaneous Application - Clinical Programming or Biostatistics
Contribute to clinical programming or biostatistics work across studies, applying CDISC standards and statistical methods to deliver reliable data and support high-quality biometrics projects.
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