The role involves providing statistical expertise and scientific leadership while working cross-functionally on pharmacometric analysis. You will be responsible for developing PopPK/PD datasets and ensuring compliance, quality, and governance in clinical trial data.
The Senior Statistician will lead statistical aspects of clinical trials, including the creation of Statistical Analysis Plans and oversight of study documentation. They will also act as a global lead across multiple studies, providing mentorship to junior staff and supporting regulatory interactions.
The role involves managing clinical and non-clinical trial data, including eCRF programming, user acceptance testing, and clinical coding. The coordinator will also act as a lead data manager for non-complex studies and ensure the production of clean, high-quality databases.
The Clinical Data Coordinator will manage clinical trial data, including eCRF programming, edit checks, and clinical coding to ensure database cleanliness. They will also act as a Lead Data Manager for non-complex studies and contribute to process improvements within the study team.
The principal programmer will lead programming activities across clinical and non-clinical studies, ensuring high-quality dataset production and regulatory submission support. They will also provide scientific leadership, oversee CRO deliverables, and drive quality control strategies.
The role involves providing statistical expertise and scientific leadership while supporting global pharmaceutical clients. Responsibilities include delivering high-quality analytical outputs, reviewing complex statistical analysis plans, and fostering people development.
The Senior Data Anonymization Programmer will provide expert programming for clinical data anonymization and regulatory disclosure activities. Responsibilities include developing complex macros, performing quality control on outputs, and ensuring compliance with SDTM and ADaM standards.
The Principal Programmer will lead clinical and non-clinical study programming activities, ensuring high-quality dataset production and regulatory compliance. They will provide scientific leadership, manage complex macros, and oversee the development of statistical analysis plans and regulatory documentation.
The role involves providing scientific leadership and statistical programming expertise to support cross-functional teams in clinical trials. Responsibilities include developing PopPK/PD datasets, ensuring compliance and quality, and contributing to e-submission packages.
The Principal Programmer will lead studies and provide statistical and scientific leadership for global pharmaceutical clients. The role involves hands-on programming using R and SAS while potentially managing other team members.
The senior data operations programmer will develop and maintain clinical trial databases, including eCRFs, edit checks, and custom functions. They will also participate in study setup, perform senior reviews of database specifications, and ensure the deployment of non-eCRF technologies.
The role involves providing scientific leadership and statistical expertise to support global pharmaceutical clients. Responsibilities include leading independent analyses, ensuring compliance with regulatory standards, and fostering team development.
The Group Financial Controller is responsible for the integrity of financial reporting, controls, and cash management while leading month-end and year-end processes. They also partner with the CFO on M&A activities, commercial contracting, and strategic value creation.
The Senior Statistician will provide scientific leadership and statistical expertise for vaccine and MPD studies. They are responsible for ensuring compliance, quality, and governance while mentoring team members.
The principal programmer will lead programming activities across clinical and non-clinical studies, ensuring high-quality dataset production and regulatory submission support. Responsibilities include providing scientific leadership, managing QC strategies, and overseeing CRO deliverables.
The Principal Statistician will provide scientific leadership and statistical expertise for GI studies while supporting a global pharmaceutical client. Responsibilities include developing post-hoc analysis plans, ensuring compliance and quality, and mentoring team members.
The Principal Programmer will lead clinical and non-clinical study programming, ensuring high-quality dataset production and regulatory submission compliance. They will provide scientific leadership, mentor team members, and manage complex programming tasks while adhering to project timelines.
The Senior Statistician will lead statistical aspects of clinical trials, including the development of Statistical Analysis Plans and study documentation. They will oversee reporting teams, provide scientific leadership, and act as a consultant for pharmaceutical and biotech clients.
The Principal Statistician will provide technical support and scientific leadership for Neuroscience studies within a CRO environment. Responsibilities include managing study leads, ensuring compliance and quality, and mentoring team members.
The role involves providing statistical expertise and scientific leadership while overseeing people development and governance. You will support complex oncology clinical trials by ensuring compliance and high-quality programming standards.
Develop and maintain trial-specific databases, including eCRFs and edit checks, while adhering to project timelines. Support the programming of reports and listings to ensure standardization for data review and analysis.
The candidate will program and validate complex datasets, SDTMs, and non-efficacy outputs for oncology studies. They will also lead programming teams, develop standard macro libraries, and ensure compliance with SOPs and regulatory requirements.
The role involves providing statistical expertise and scientific leadership for pharmaceutical studies in areas such as oncology, GI, neuroscience, or infectious diseases. Responsibilities include managing compliance, quality, governance, and people development.
Provide statistical expertise and scientific leadership for global pharmaceutical clients focusing on GI, oncology, neuroscience, or infectious disease studies. Responsibilities include authoring SAP/TLF shells and validating ADaM/TLFs for DMC, IA, and CSR.
Lead and deliver SDTM mapping and conversion activities for Real-World Data to CDISC standards. Act as a Subject Matter Expert to develop ECRT packages and collaborate cross-functionally to ensure quality delivery.
Lead studies and manage sponsor systems by programming and validating complex datasets and SDTMs. Act as a lead programmer across multiple studies, ensuring quality delivery and coordinating with statisticians and project managers.
