The Senior Clinical Data Coordinator will lead clinical coding activities, manage third-party data, and oversee database set-up and validation for clinical trials. They will act as the lead Data Manager, collaborating with sponsors and suppliers to ensure project deliverables meet quality and timeline standards.
The programmer will work on clinical and non-clinical trials by producing high-quality datasets and outputs while adhering to project timelines. Responsibilities include maintaining CDISC standards, creating macros, and providing statistical and scientific leadership.
Lead data management for assigned clinical and non-clinical studies, including eCRF and database production and validation, clinical coding, and third-party data management. Coordinate with sponsors and suppliers to deliver clean databases on schedule while maintaining quality and supporting team development and process improvement.
Coordinate data management activities for clinical and non-clinical trials, including eCRF specification and testing, data review, clinical coding, third-party data management, and query resolution. Deliver data management documentation and reports, maintain clean databases, and lead data management for assigned non-complex studies.
Develop and maintain trial-specific databases, including eCRFs and edit checks, while ensuring compliance with CDASH and SDTM standards. Support the programming of reports and listings to facilitate data review and analysis for external partners.
The Senior Clinical Data Coordinator will act as the lead Data Manager for assigned studies, ensuring the quality and timely delivery of clinical data management activities. They will also mentor less experienced team members and maintain strong relationships with internal and external stakeholders.
The senior programmer will produce complex datasets and outputs for clinical and non-clinical trials while adhering to strict timelines. They are responsible for creating and debugging complex macros, reviewing data specifications, and providing scientific leadership within the team.
The FSP Manager serves as the primary point of contact between Phastar and the client, overseeing staffing and account needs. They provide scientific leadership, statistical expertise, and ensure compliance and quality across clinical trial projects.
The senior programmer will produce complex datasets and outputs for clinical and non-clinical trials while adhering to strict deliverable timelines. They will also provide scientific leadership, ensure compliance and quality, and collaborate with cross-functional teams including statisticians and data management.
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 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 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 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 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 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 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 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 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 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 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 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 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 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.
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.
