474 Sas Programming Jobs - Page 6

As a Business Analyst at Citi's Operations Analytics team within the Citi AIM vertical, your role involves leveraging data analysis to enhance efficiency, reduce costs, and improve customer experience across the front and back office. You will work on optimizing contact center performance, automating processes, resolving customer issues, and supporting KYC operations. Your goal is to drive data-driven decision-making for operational improvements. **Key Responsibilities:** - Conduct in-depth analyses of current operational processes to identify inefficiencies and areas for improvement. - Utilize expertise in data management principles, SQL, SAS programming for data extraction, manipulation, a...

Support business and analytics stakeholders Solve open-ended,business problems basic to advanced analytics hands-on to derive insights from data and/or automate critical processes using analytical techniques Required Candidate profile hands on Exp in SQL and SAS with Open Source Tools build queries for data extraction hands-on exp of latest Analytics Data Visualisation tools Exp in credit card or financial services industry

Role Overview: As a Lead Statistical Programmer, you will be responsible for overseeing programming activities for clinical trials, regulatory submissions, and integrated analyses. Your role will involve leading a team, ensuring high-quality deliverables, and developing efficient programming standards to support drug development. Key Responsibilities: - Lead statistical programming activities for a compound or therapeutic area. - Manage, mentor, and guide a team of statistical programmers. - Create and validate analysis data sets (ADaM), tables, listings, and figures (TFLs) following CDISC standards. - Develop and validate Integrated Summary of Safety (ISS) and Integrated Summary of Efficacy...

As a Manager, Analytics - H&W Platform at Synchrony, your role will involve supporting the Health & Wellness platform business and analytics stakeholders in making informed decisions through data, analytics, and insights. You will proactively discover, lead, and solve open-ended/ambiguous business problems using basic to advanced analytics/data science tools and techniques. Your responsibilities will include deriving insights from data, automating critical processes, ensuring timely delivery, accuracy, and documentation, and contributing to internal initiatives and special projects as assigned. Key Responsibilities: - Support Health & Wellness platform business and analytics stakeholders in ...

Role Overview: As a Lead Statistical Programmer in the clinical data field, you will be responsible for overseeing programming activities related to clinical trials, regulatory submissions, and integrated analyses. Your role will involve leading a team, ensuring the delivery of high-quality work, and establishing efficient programming standards to support drug development. Key Responsibilities: - Lead statistical programming activities for a compound or therapeutic area. - Manage, mentor, and guide a team of statistical programmers. - Create and validate analysis data sets (ADaM), tables, listings, and figures (TFLs) following CDISC standards. - Develop and validate Integrated Summary of Saf...

Designation: Clinical Data Manager Full Time Opportunity Job Description: - Tasks have been carried out independently and the status is communicated back to all relevant parties. - Ensuring that the electronic data generated is transferred to the customer as per the Data Specifications - Configure, QC, and Test Study EDT and obtain client sign off on approved DTS. - Ensure EDT is delivered in accordance with the required frequency and specifications. - Control the receipt and integration of partner or 3PL data, as per scope of study. - Perform data reconciliations within the context of the assigned team, [and service], as appropriate to ensure a clean data set. - Perform approved data cleani...

Designation: Clinical Data Manager Full Time Opportunity Location: Full Time Job Description: - Tasks have been carried out independently and the status is communicated back to all relevant parties. - Ensuring that the electronic data generated is transferred to the customer as per the Data Specifications - Configure, QC, and Test Study EDT and obtain client sign off on approved DTS. - Ensure EDT is delivered in accordance with the required frequency and specifications. - Control the receipt and integration of partner or 3PL data, as per scope of study. - Perform data reconciliations within the context of the assigned team, [and service], as appropriate to ensure a clean data set. - Perform ...

As a Statistical Programmer working fully embedded within one of our pharmaceutical clients, you will be at the heart of our client's innovation, with the support of Cytel right behind you. You will be dedicated to one of our global pharmaceutical clients, contributing to the advancement of patient treatment and working with autonomy and ownership. This role presents an exciting opportunity to be a part of a new program. Your responsibilities as a Statistical Programmer will include: - Performing data manipulation, analysis, and reporting of clinical trial data using SAS programming - Creating and validating datasets/analysis files, tables, listings, and figures (TLFs) with SAS programming s...

Role Overview: As a Statistical Programmer II at Syneos Health, you will be part of a leading fully integrated biopharmaceutical solutions organization dedicated to accelerating customer success. Our Clinical Development model prioritizes putting the customer and patient at the center of our work, aiming to simplify processes and innovate as a team to make a difference in people's lives. Key Responsibilities: - Utilize advanced proficiency in Base SAS, SAS Macro, and SAS SQL for clinical trial data analysis and reporting - Demonstrate in-depth knowledge of CDISC standards to develop ADaM specifications and datasets for regulatory submissions - Produce high-quality Tables, Listings, and Figur...

As a Data Analyst at our company, your role will involve building and maintaining data aggregation processes and dashboards. You will create interactive and compelling visual, numeric, and written summaries. Ensuring that data governance policies are followed will be a key responsibility, along with training and coaching business users on BI tools. Promoting data literacy and a self-serve culture across the enterprise will also be a focus area. Additionally, you will analyze business intelligence data to inform business and product decisions. You will blend historical data from various sources and identify trends in the industry and competitor strategies. Collaborating with other business ar...

Proficient in creating complex queries in SAS and SQL Proficient in writing SAS and SQL codes using industry best practices Good knowledge of Relational Data Base Management and SQL, SAS (expertise), Good to have- SSIS, Power BI or any other BI Tools Superior analytical and problem solving skills Should be able to work on a problem independently and prepare client ready deliverable with minimal or no supervision Good communication skill for client interaction Strong ability to translate functional specifications / requirements to technical requirements Insurance domain knowledge would be good to have Interested candidates can share their resumes on nishi@jobpoint.co.in

- Tasks have been carried out independently and the status is communicated back to all relevant parties. - Ensuring that the electronic data generated is transferred to the customer as per the Data Specifications - Configure, QC, and Test Study EDT and obtain client sign off on approved DTS. - Ensure EDT is delivered in accordance with the required frequency and specifications. - Control the receipt and integration of partner or 3PL data, as per scope of study. - Perform data reconciliations within the context of the assigned team, [and service], as appropriate to ensure a clean data set. - Perform approved data cleaning functions in order to maintain a clean data set. - Adherence to all wri...

ISS - Senior Statistical Programmer - India ICON plc is a world-leading healthcare intelligence and clinical research organization. We re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Senior Statistical Programmer I to join our diverse and dynamic team. As a Senior Statistical Programmer I at ICON, you will play a crucial role in analyzing clinical trial data and supporting the statistical analysis process to ensure high-quality results. You will contribute to the success of our clinical studies by developing and validating statistical programs, co...

ISS - Senior Statistical Programmer - India ICON plc is a world-leading healthcare intelligence and clinical research organization. We re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Senior Statistical Programmer I to join our diverse and dynamic team. As a Senior Statistical Programmer I at ICON, you will play a crucial role in analyzing clinical trial data and supporting the statistical analysis process to ensure high-quality results. You will contribute to the success of our clinical studies by developing and validating statistical programs, co...

You will be part of our team as a Senior SAS Programmer, where you will be responsible for providing SAS programming support for TFL generation and offering statistical/programming inputs for CRF design and review. Additionally, you will be involved in developing and validating standard and ad-hoc SAS macros. You will carry out reviews of CRF and aCRF, statistical analysis plans, and programming specifications for efficacy variables. Validating Safety Tables using SAS and ensuring the validation of ADaM and derived datasets will also be part of your responsibilities. Furthermore, you will be involved in validating SDTM datasets and their specifications while adhering to the required training...

Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, youll be at the heart of our clients innovation. As a Senior Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program. Position Overview: As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials. This role can be performed...

As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials. This role can be performed as fully remote. Our values We believe in applying scientific rigor to reveal the full promise inherent in data. We nurture intellectual curiosity and encourage everyone to approach new challenges with enthusiasm and the desire for discovery. We believe in collaboration and invite a diversity of perspectives, drawing on a variety of talents to create a wealth of possibilities. We prize innovation and seek intelligent solutions using leading-edge technology. Here at Cyte...

Job description Job Summary We are seeking a skilled In Vitro Statistician with 5 - 10 years of experience to support our research and development teams in statistical analysis of in vitro studies. The ideal candidate will be responsible for designing experiments, analyzing data, and providing statistical insights to support decision-making in pharmaceutical, biotechnology, or life sciences research. Key Responsibilities: Design, develop, and analyze in vitro study experiments, ensuring statistical rigor and accuracy. Apply appropriate statistical models and methodologies for data interpretation. Work closely with scientists, biologists, and researchers to provide statistical guidance in stu...

Educational Requirements Bachelor of Engineering Service Line Data & Analytics Unit Responsibilities The ideal candidate will have expertise in developing software applications using SAS and Python. Roles and Responsibility Design, develop, and test software applications using SAS and Python. Collaborate with cross-functional teams to identify and prioritize project requirements. Develop and maintain large-scale data processing systems using SAS and Python. Troubleshoot and resolve technical issues efficiently. Participate in code reviews and contribute to improving overall code quality. Stay updated with industry trends and emerging technologies in SAS and Python. Job Requirements Strong pr...

About The Role JR: R00208204 Experience: 10-12Years Educational Qualification: Any Degree --------------------------------------------------------------------- Job Title - S&C- Data and AI - CFO&EV Quantexa Platform(Assoc Manager) Management Level: 8-Associate Manager Location: Pune, PDC2C Must-have skills: Quantexa Platform Good to have skills: Experience in financial modeling, valuation techniques, and deal structuring. Job Summary : This role involves driving strategic initiatives, managing business transformations, and leveraging industry expertise to create value-driven solutions. Roles & Responsibilities: Provide strategic advisory services, conduct market research, and develop data-dr...

Dear Candidate, Below are the Job Details for Clinical SAS Programmer role at CBCC Global Research LLP. Candidate should have the exposure of SDTM, ADAM and TLF. Job Location : Ahmedabad At Office Position : 2 Experience: 2-5 years in CRO preferred / Pharma industry Qualification : M. Sc. Statistics/Any Science Graduate Mandatory experience in Clinical trials Responsibilities: Ensure consistently high quality outputs for reporting and submission- 1.1. Build SAS datasets from clinical database. 1.2. Develop SAS macros, templates and utilities for data cleaning and reporting. 1.3. Utilize SDTM guidelines to build datasets. 1.4. Communicate with an internal team to create deliverables for pharm...

As a Statistical Programmer II at Advanced Clinical, you will play a crucial role in providing programming support for clinical trials. Your responsibilities will include exceeding the expectations and responsibilities of a Statistical Programmer I, understanding and implementing CDISC and other regulatory standards, and following internal SAS programming conventions. You may also serve as a programming lead, prepare programming specifications for SDTM, ADaM, and other derived datasets, and work with cross-functional team members to ensure accurate and high-quality statistical outputs. In this role, you will apply your knowledge of SAS programming to program and develop statistical outputs a...

The Senior Statistical Programmer II will be a primary resource for the development and validation of programs that create datasets conforming to Alexion and CDISC standards, as well as Tables, Listings, and Figures ( TLFs ) for analysis purposes. Depending on the size and complexity of a study, they may act as the lead programmer for the project. They will develop specifications to ensure that statistical programming elements align with the overall deliverable and ensure adherence to ICH guidelines, Good Clinical Practices, and regulatory requirements. They may act as the Programming Lead and represent Statistical Programming in meetings with internal and external clients and cross-function...

The Clinical Data Associate II role involves providing data management support for clinical trial projects from study initiation to post-database lock, while adhering to SOPs, regulatory guidelines, and study-specific plans. Your responsibilities include supporting the Lead DM, performing data entry, quality control, developing CRF specifications, building and testing clinical databases, and maintaining data management documentation. You will also be involved in training clinical research personnel, reviewing and querying trial data, conducting medical coding, and assisting with various data-related activities such as SAE/AE reconciliation and vendor coordination. Additionally, you may contr...

Good Clinical Domain knowledge with understanding of clinical phases and Work experience must be in clinical / healthcare domain. Experience in Edit Check Listings programming using SAS. 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, Reading Raw data files, creating data structures, Handling programming errors, Accessing and Managing data, Appending, Concatenating of SAS data sets. Comprehensively prepared reports using SAS report generating procedures like PROC PRINT, PROC FREQ, PROC MEANS, PROC TRANSPOSE and PROC SQL. Well versed with coding in Macros and S...