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The Executive Consultant will lead strategic consulting in Quantitative Clinical Pharmacology, mentor teams, and engage with clients for business development and scientific expertise.

The role involves programming and quality control of NONMEM PK/PD datasets, ensuring data accuracy, communication with departments, and QC of R packages.

The Senior Clinical Data Manager oversees clinical data management from study start-up to database lock, ensuring compliance, managing vendor activities, and maintaining data quality across multiple programs and CROs.

As a Senior Statistical Programmer, you will perform data manipulation, analysis, and reporting of clinical trial data using SAS, while leading or supporting multiple clinical trials within the pharmaceutical sector.

As a Principal Pharmacometrician, you will lead quantitative pharmacology activities in clinical studies, perform PK/PD modeling, and provide analytical support for trials with a focus on collaboration and regulatory strategy.

The Senior Statistical Programmer will support Phase I-IV clinical trials using SAS for data analysis, reporting, and validation, while ensuring CDISC standards are met and collaborating with cross-functional teams.

The Tools and Standards Specialist will develop and maintain R-based solutions, automate data processes, and implement CDISC-compliant workflows, while supporting innovation and improving existing processes.

As a Senior Statistical Programmer, you'll manage clinical trial data, generate and validate datasets, and communicate with cross-functional teams within the pharmaceutical industry.

The Senior Biostatistician supports clinical studies, develops study protocols, performs statistical analyses, prepares clinical reports, and ensures compliance with FDA regulations.

The Principal Statistical Programmer will generate SDTM/ADaM files, develop SAS programs for clinical trials, oversee CRO deliverables, and ensure compliance with FDA regulations.