The role involves providing scientific leadership and statistical expertise while producing complex datasets and outputs for clinical and non-clinical trials. You will be responsible for developing data specifications, creating macros, and ensuring compliance and quality across all programming activities.
The Senior Clinical Data Coordinator will lead clinical coding activities, manage third-party data, and act as the lead Data Manager for assigned studies. They are responsible for producing and validating eCRFs and databases while ensuring compliance with deliverable timelines and quality standards.
The principal programmer will lead programming activities across clinical studies, ensuring high-quality dataset production and regulatory submission support. They will also provide scientific leadership, mentor team members, and ensure compliance with industry standards.
The senior programmer will produce complex datasets and outputs for clinical and non-clinical trials while adhering to strict timelines. They are responsible for providing statistical expertise, scientific leadership, and ensuring compliance and quality across all programming activities.
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, mentor team members, and ensure compliance with industry standards.
The principal programmer will lead programming activities across clinical and non-clinical studies, ensuring high-quality dataset production and regulatory submission support. They are responsible for providing scientific leadership, managing complex macros, and reviewing statistical analysis plans.
The role involves working as a programmer on clinical and non-clinical trials to produce datasets and outputs while adhering to quality and timeline standards. Responsibilities include maintaining CDISC standards, creating macros, and providing scientific leadership within the team.
The senior programmer will produce complex datasets and outputs for clinical and non-clinical trials while adhering to strict deliverable timelines. They will provide scientific leadership, ensure compliance and quality, and collaborate effectively with cross-functional teams.
The Principal Statistician will provide scientific leadership and statistical expertise for oncology-focused observational studies. They will also manage projects, develop statistical analysis plans, and support evidence generation activities while collaborating with global teams.
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 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 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 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 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 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 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 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 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 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 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 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.
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 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.
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.
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.
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.
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.
