Statistical Programmer

**Department-** Biostatistics - CDS GBS **The Position**: The Statistical Programmer will be responsible for statistical programming and reviewing SAS programmes in the designated clinical trial. Additionally, the Statistical Programmer is accountable for: - CRF (Case report form), TVP (Trial Validation Plan), and data flow plan input and Programming of...

Summary Of Position: • Key contributor responsible for quality, timely and cost efficient execution of all statistical programming aspects of assigned studies or project-level activities • Customary point of contact for Trial Statisticians and other members of the Clinical Trial Team Key Responsibilities: • Lead statistical programming...

**Career level C**: **Statistical Programmer**: **Play a critical role in making our pipeline accessible to patients** **AstraZeneca** is a global, science-led, patient-oriented biopharmaceutical company that focuses on the discovery, development, and commercialization of prescription medicines for some of the world’s most serious diseases. But we’re...

Summary Of Position:• Key contributor responsible for quality, timely and cost efficient execution of all statistical programming aspects of assigned studies or project-level activities• Customary point of contact for Trial Statisticians and other members of the Clinical Trial TeamKey Responsibilities:• Lead statistical programming activities as...

Company Description Ergomed PLC is a rapidly expanding full service mid-sized CRO specialising in Oncology and Rare Disease. Since its foundation in 1997 the company has grown organically and steadily by making strategic investments and landmark acquisitions, with operations in Europe, North America and Asia Our company allows for employee visibility (you...

**Description** **Statistical Programmer II** Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide practical value to help our...

Summary: Key contributor responsible for statistical programming of deliverables for assigned studies or project-level activities under guidance of a Trial Programmer. Major Accountabilities: - Create primary program to generate deliverables in accordance with TFL shells, programming instructions and programming dataset specifications - Validate...

We are GREAT PLACE TO WORK - CERTIFIED Summary of Position: - Key contributor responsible for statistical programming of deliverables for assigned studies or project-level activities under guidance of a Trial Programmer. - Key Responsibilities: - Create primary program to generate deliverables in accordance with TFL shells, programming, instructions and...

Key Skills :Statistical Programming: Proficient in SAS, R, and other statistical software.Clinical Trials: Extensive experience in clinical trial design, analysis, and reporting.Data Management: Data validation, cleaning, and integration.Regulatory Compliance: Knowledge of FDA and EMA guidelines.Programming Languages: SAS, R, Python.Statistical Analysis:...

Key Skills : Statistical Programming: Proficient in SAS, R, and other statistical software. Clinical Trials: Extensive experience in clinical trial design, analysis, and reporting. Data Management: Data validation, cleaning, and integration. Regulatory Compliance: Knowledge of FDA and EMA guidelines. Programming Languages: SAS, R, Python. Statistical...

Key Skills :Statistical Programming: Proficient in SAS, R, and other statistical software.Clinical Trials: Extensive experience in clinical trial design, analysis, and reporting.Data Management: Data validation, cleaning, and integration.Regulatory Compliance: Knowledge of FDA and EMA guidelines.Programming Languages: SAS, R, Python.Statistical Analysis:...

Company Description Ergomed PLC is a rapidly expanding full service mid-sized CRO specialising in Oncology and Rare Disease. Since its foundation in 1997 the company has grown organically and steadily by making strategic investments and landmark acquisitions, with operations in Europe, North America and Asia Our company allows for employee visibility (you...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

Principal Duties ResponsibilitiesPerform and implement, under supervision,the following for clinical studies: (i) the SAS programming, testing, anddocumentation of statistical programs for use in creating statisticaltables, figures, listings, and graphs and (ii) the programming of analysisdatasets (derived datasets) and transfer filesfor internal and...

Principal Duties & ResponsibilitiesPerform and implement, under supervision, the following for clinical studies: (i) the SAS programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, listings, and graphs and (ii) the programming of analysis datasets (derived datasets) and transfer files for internal...

A career at our company is an ongoing journey of discovery: our 58,000 people are shaping how the world lives, works and plays through next generation advancements in Healthcare, Life Science and Electronics. For more than 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of...

Principal Duties & Responsibilities Perform and implement, under supervision, the following for clinical studies: (i) the SAS programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, listings, and graphs and (ii) the programming of analysis datasets (derived datasets) and transfer files for...

Overview: Work as a principal programmer across multiple clinical and non-clinical studies; supporting regulatory submission activities; producing and validating datasets and outputs to excellent quality whilst adhering to deliverable timelines. Excellent knowledge of CDISC SDTM and ADaM implementation guidelines working independently in this area;...

Principal DutiesResponsibilitiesPerform and implement under supervision the following forclinical studies: (i) the SAS programming testing and documentationof statistical programs for use in creating statistical tablesfigures listings and graphs and (ii) the programming of analysisdatasets (derived datasets) and transfer filesfor internal andexternal clients...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...