Sas Programmer

**Brief Position Description**: The Clinical Data Programmer SAS is responsible for data analysis and business intelligence activities related to study related clinical and operational data for the purpose of facilitating clinical data inspection and quality control, as well as operational performance control of clinical sites by creating reports,...

Good Clinical Domain knowledge with understanding of clinical phases and Work experience must be in clinical / healthcare domain. Experience in Clinical SAS Programming Experience in Data Import Programming using SAS, SAS Output Delivery system (ODS) for generating reports in specific output formats like RTF, PDF, and HTML. Handling missing values,...

**About the role**: The Clinical Data Programmer SAS III (must be SAS Certified) is responsible for data analysis and business intelligence activities related to study related clinical and operational data for the purpose of facilitating clinical data inspection and quality control, as well as operational performance control of clinical sites by creating...

**Minimum Qualifications & Experience**: - Must be SAS Certified - Graduate in computer science, data science, mathematics, or life science related field, or similar. - A minimum of 5 years of experience in a role related to business intelligence, data science, data analysis, and clinical data management or clinical data programming in a pharmaceutical...

**Minimum Qualifications & Experience**: - Graduate in computer science, data science, mathematics, or life science related field, or similar. - A minimum of 2 years of experience in a role related to business intelligence, data science, data analysis, and clinical data management or clinical data programming in a pharmaceutical company, CRO or EDC software...

-Job description **Business**:MSS **Open positions: 1** **Role Title**:FRTB SA - Regulatory Applications Co-Ordinator **Global Career Band**:Grade **4 **Location **_(Country / City)_**:I**ndia/Bangalore **The Opportunity**: This role sits within the FRTB Programme Team as the SA Applications Co-ordinator globally. The jobholder is expected to work...

**Job Title: Clinical Programmer** **Career Level - C** **Skills required - **SAS, SQL, PowerBI, Python, MicroStrategy **Introduction to Role**: Are you ready to take a crucial inter-disciplinary approach to save patients' lives? As a Clinical Programmer, you will be primarily responsible for providing support to activities related to programming,...

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...

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:...

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...

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...

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 & 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...

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...

Development and implementation of solutions to global technical service issues and concerns regarding EDC tools like Medidata RAVE, Oracle InForm, Veeva and SAS programming. - Read, understand and program EDC objects/SAS programming as per the specification documents which meets client requirements and projects. - Perform any post production changes to the...

Key Responsibilities: - Generate standard and custom Trial Monitoring reports to support Risk Based Monitoring (RBM) across the trial portfolio. - Prepare and maintain report-related documentation. - Participate in Trial Monitoring report meetings. Main Job Tasks: - Understand stakeholder needs for Trial/Medical Monitoring and Risk Indicator reports and...

**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 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...