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Biotech • Pharmaceutical
Develop and QC tables, figures, listings and derived datasets for RWE projects using SAS and SQL. Extract, manipulate, and manage large longitudinal healthcare datasets (claims, EMRs), optimize SAS macros, collaborate with Outcomes Research teams, mentor junior programmers, and follow project management procedures to deliver high-quality, reproducible results.
Biotech • Pharmaceutical
As a Statistical Programmer I, support statistical and programming teams in clinical trial reporting, generating datasets, and reviewing analysis plans while learning SAS programming.
Biotech • Pharmaceutical
The Senior Programmer III will produce and validate datasets using SAS, mentor junior programmers, and ensure quality in clinical trial data management.
Biotech • Pharmaceutical
As a Senior Programmer III, you will lead clinical programming efforts, support junior programmers, develop datasets using SAS, and ensure compliance with CDISC standards.
Biotech • Pharmaceutical
The Digital Marketing Executive will manage multi-channel campaigns, enhance brand visibility, oversee website content, and analyze campaign performance. Responsibilities include email marketing, social media management, and event planning to drive engagement and support business growth.
Biotech • Pharmaceutical
Senior statistical programmer responsible for designing and analyzing clinical studies, producing and QCing CDISC-compliant datasets and TLFs, providing peer review, ensuring regulatory compliance, managing project work and mentoring team members, and liaising with sponsors and lead statisticians.
Biotech • Pharmaceutical
The Principal Statistician leads statistical support for clinical trials, develops statistical models, and mentors junior statisticians while ensuring high-quality deliverables.
Biotech • Pharmaceutical
The role involves supporting regulatory safety activities in Turkey, ensuring compliance with pharmacovigilance reporting requirements, and collaborating with local health authorities. Responsibilities include preparing safety reports, translating documents, and providing pharmacovigilance support to teams.






