Oncology Clinical Trials Statistical Programming Expert

Statistical Programmer RoleWe are seeking an experienced Statistical Programmer to join our team in Oncology research. As a key member of our global team, you will play a vital role in developing and maintaining ADaM datasets, TLFs, and other analytical outputs for clinical trials.Key Responsibilities:ADaM Dataset Development: Develop, validate, and maintain...

Key Responsibilities Develop, validate, and maintain ADa M datasets , TLFs , and other analytical outputs for clinical trials. Support Oncology studies by ensuring accuracy, consistency, and regulatory compliance in all programming deliverables. Contribute to ISS/ISE activities , including dataset integration, analysis, and documentation. Work closely with...

Job Title: Senior Statistical ProgrammerThis role requires a highly skilled statistical programmer to lead and execute the full spectrum of statistical programming deliverables. The ideal candidate will have expertise in SAS and R, with experience working on clinical trial datasets and outputs.Key Responsibilities:Program, validate and maintain clinical...

Lead Statistical ProgrammerSponsor-dedicated statistical programming expert working within a pharmaceutical client environment, supported by Cytel.This is an exciting time to be part of this new program.Key Responsibilities:Develop and deliver SDTM, ADaM specifications, datasets, reviewer's guide, and define.xml files for multiple studiesCreate SAS programs...

Job OpportunityThe ideal candidate should possess extensive experience in statistical analysis and reporting within the context of clinical trials, showcasing proficiency in SAS and R programming languages, as well as an ability to collaborate closely with programming and clinical teams.Main Responsibilities:Statistical analysis and modelingData...

**Job Summary**: **Responsibilities**: **Protocol Development**: Collaborate in the development of clinical trial protocols, ensuring alignment with regulatory requirements and study objectives. Provide input into the design of study documents, such as Case Report Forms (CRFs) and Informed Consent Forms (ICFs). **Site Selection and Monitoring**: Conduct...

Job Title: Lead Programmer and Data AnalystJob Description:The Senior Programmer II position involves providing expert programming support to various departments across multiple projects. The successful candidate will work with large databases, generate reports, and assist analysts in exploring real-world healthcare data assets.This role requires excellent...

Job Title: Quality Assurance AuditorWe are seeking a highly skilled Quality Assurance Auditor to ensure compliance and quality at Clinical Trial sites.Audits of clinical research sites across phases I–IV will be conducted.Clinical Research Forms, informed consent forms, and regulatory documents will be reviewed.Audit findings will be identified and...

Are you a detail-oriented professional with excellent analytical skills? We are seeking a Clinical Site Auditor to ensure compliance and quality at clinical trial sites.This role involves conducting site audits, reviewing documentation, and verifying adherence to protocols, GCP, GLP, and regulatory requirements.Key Responsibilities:Conduct audits of clinical...

Job SummaryThe Global Lead Statistical Programmer will lead statistical programming activities for therapeutic areas or compounds/indications within multiple studies/projects.Develop and maintain Programming Standards following industry guidelines.Create CDISC Standard Mappings and specifications for SDTM and ADaM datasets.Develop and oversee the development...