Clinical 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...

**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,...

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...

Associate Clinical Data Programmer **Category**:Data & AI**Location**:Bangalore, Karnataka, IN**Department**:Data Systems & Automation, Bangalore Global Development- **About the department** - Data Systems & Automation, Bangalore Global Development GBS is one of the most competent and diverse team of professionals who are mainly responsible for providing...

**Description** **Principal Statistical Programmer** 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...

**Department**:Data Systems & Automation, Clinical & Data Science (CDS) GBS** **About the department** Data Systems & Automation, Bangalore Global Development is one of the most competent and diverse team of professionals who are mainly responsible for providing functional and system support to execute clinical trials across Product Development Plan...

**OVERVIEW** Statistical Programmers will work with Principal Technical Consultant to provide SAS programming expertise in data extracted from various databases. Statistical Programmers document and program for the transformation of raw data to Study Data Tabulation Model (SDTM) datasets, Analysis Data Model (ADaM) datasets, and develop programming to...

**Responsibilities**: - Collaborate with cross-functional teams, including biostatisticians, data managers, and clinical research associates, to develop programming specifications and data analysis plans. - Design and develop SAS programs to generate tables, listings, and graphs (TLGs) for clinical study reports, regulatory submissions, and other...

**Department**:Data Systems & Automation, Clinical & Data Science (CDS) GBS **About the department** Data Systems & Automation, Bangalore Global Development is one of the most competent and diverse team of professionals who are mainly responsible for providing functional and system support to execute clinical trials across Product Development Plan...

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...

**Minimum Experience Required: 1-5 years** Main Responsibilities and Accountabilities: - Ensures that data from multiple source systems is pulled integrated into datasets that support the creation of data visualizations - Collaborates in the development of strategies for the integration of non eCRF data in the eCRF database (eg, IRT integration) provides...

Location: Mumbai, Chennai, Bangalore, Hyderabad, Ahemedabad,Delhi NCRAbout the Client:we have retained with CMMI level 4 client with the position of Banking operations for the level of SPE.Client is a global IT solutions company specializing in delivering simple and scalable solutions to address complexbusiness than 1,500 staff delivers technical and domain...

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...

Senior/Lead Statistical Programmer Full-Time Bengaluru, Karnataka, India Hyderabad, Telangana, India Description Job Responsibilities: • Annotate Case Report Form ( following FDA/CDISC or sponsor guidelines. • Develop SDTM specifications and generate SDTM datasets using SAS. • Develop ADaM specifications and generate ADaM datasets...