351 Sas Programming Jobs

Role Overview: As AVP, Remediation Analytics at Synchrony, you will have the opportunity to work on major remediation projects with special focus on Credit functions. Your responsibilities will include understanding business requirements, building complex logics to identify and remediate the impacted population, and managing various projects within the framework of remediation analytics. Key Responsibilities: - Develop Advanced SAS and/or SQL code, visual basic macros or other query tools for remediation. - Support remediation projects by partnering with FRCs and cross-functional teams, understanding business requirements, and developing analytics solutions to identify impacted population and harm. - Timely escalate to manager if roadblocks are encountered, work with manager and leadership to resolve roadblocks for the project. - Minimize defects by utilizing standard code sets and waterfalls, ensuring all certification and validation requirements are completed prior to submission, and correcting defects found timely. - Support audits via documentation of code and analytic outcomes and extraction of data. - Ensure quality of deliverables by implementing controls to ensure accuracy. - Work on multiple projects simultaneously, establishing priorities and coordinating work. - Analyze remediation analytic processes and technology, and present recommendations for improvement. - Support Best-in-class analytic solutions/algorithms, provide insight and support in various initiatives/projects. - Share critical experiences and best practices across the Remediation COE, provide updates on project progression, and escalate challenges and roadblocks timely. - Perform other duties and/or special projects as assigned. Qualifications Required: - Bachelor's degree and minimum 5 years of experience in a consumer finance & banking organization, or in lieu of a degree, 7+ years of experience in a consumer finance organization. - 4+ years of experience in Analytics domain. - Minimum 4 years of SAS programming experience. - Solid working knowledge of Unix and Excel. - Strong written/oral communication skills. - Able to work hours that compliment US, not necessarily match but have some degree of overlap. Additional Details of the Company: Synchrony is a premier consumer financial services company delivering a complete digitally enabled product suite across various industries. The company has been recognized for its commitment to employee well-being, career advancement, and diversity. Grade/Level: 10 Job Family Group: Data Analytics,

As a SAS Programmer at Catalyst Clinical Research, you will play a crucial role in providing SAS programming support for Statistics and Data Management functions related to clinical trials and regulatory submissions. Your responsibilities will involve collaborating closely with Biostatisticians and Data Managers to develop SAS programs for validating tables, listings, and figures, as well as assisting with data cleaning and query generation. Additionally, you will serve as a contact for programming activities within the organization. Key Responsibilities: - Perform data manipulation techniques and advanced programming techniques such as arrays, transpositions, complex merges, SQL, SDTM, etc., and develop generic macros for generating listings, tables, and graphs. - Engage in statistical programming and validation of CDISC SDTM, Analysis Datasets (ADaM), and Tables, Listings, Graphs (TLGs). - Analyze information to devise innovative solutions for programming and data analysis challenges. - Produce high-quality results efficiently within specified time constraints. - Coordinate multiple priorities successfully and lead statistical programming activities on internal project teams. - Assist in identifying project priorities, communicating timelines, and ensuring the efficiency and quality of data reporting. - Represent the department in client meetings/presentations and maintain positive relationships with sponsors and collaborators. - Contribute to the ongoing improvement of programming processes and methodologies. - Provide guidance and advice to junior programmers, adapt to changing priorities, and fulfill ad hoc requests while performing high-level reviews on deliverables. Qualifications Required: - MSc in Biostatistics, Statistics, Computer Science, or a related field. - 5-7 years of experience in leading statistical programming activities in clinical research. - Preferred certification as a SAS Certified Candidate. - Good understanding of Clinical Trials and relevant terminologies. - Previous experience in pharmaceutical research or CRO setting. - Proficiency in statistical software packages, with a preference for SAS, and hands-on experience in developing SDTM datasets. - Strong verbal and written communication skills. - Positive attitude, willingness to learn, contribute to a team setting, and ability to successfully lead a single project. Visit CatalystCR.com to learn more about Catalyst Clinical Research and how your role as a SAS Programmer contributes to advancing clinical studies.,

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, and validations. - Comprehend process mapping and identify best automation steps in processes. - Design and develop workflows and automation logic using SAS, SQL, and Workflow tools. - Participate in testing and quality assurance to ensure high-quality solutions and successful project delivery. - Provide support to Senior Business Analysts in various project activities, including requirements gathering, process mapping, and documentation. - Effectively communicate with stakeholders, collaborate with cross-functional partners and teams. - Assist in documenting business processes, analyzing data, and preparing reports to support project decision-making. - Contribute to the development of solutions by assisting with testing, documentation, and training materials. **Qualifications:** - Work experience: 2-5 years with Masters as Educational background, 4-7 years with Bachelors as Education background - Strong analytical and problem-solving skills - Experience with process mapping and workflow automation tools - Technical Skills: Exposure in building solution designs using SQL, SAS, Xceptor, MS Excel, Tableau, and other BI tools - Coding Expertise in SAS & SQL, Autosys package - Excellent communication and interpersonal skills - Good understanding of the banking domain and banking products - Ability to multi-task effectively in a fast-paced environment - Proficient in MS Excel and PowerPoint By joining Citi, you will have the opportunity to grow your career, contribute to your community, and make a real impact. If you are passionate about leveraging data to drive operational improvements, this role at Citi may be the perfect fit for you.,

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 (ISE) reports. - Ensure accuracy and consistency across clinical studies and integrated data. - Develop, test, and implement reusable standard programs and SAS macros to automate routine tasks. - Prepare reviewer guides, data definition documents, and other materials for regulatory filings. - Collaborate with cross-functional teams including Statisticians, Clinical Data Management, Medical Writing, Regulatory, and Clinical Operations. - Accurately estimate programming efforts and ensure timely project delivery. Qualification Required: - Strong proficiency in SAS programming; experience with R preferred. - In-depth knowledge of CDISC standards (ADaM, SDTM). - Experience with regulatory submissions (FDA, EMA) and clinical study lifecycle. - Knowledge of therapeutic areas such as Oncology, Immunology, Neuroscience. - Strong communication and leadership skills to guide teams and manage stakeholders. - Ability to handle multiple priorities and deliver high-quality results under deadlines.,

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 making informed decisions through data, analytics, and insights - Proactively discover, lead, and solve open-ended/ambiguous business problems using basic to advanced analytics/data science tools and techniques - Work hands-on to derive insights from data, automate critical processes, and provide actionable recommendations - Ensure timely delivery, accuracy, and documentation in line with audit procedures - Contribute to internal initiatives, perform other duties, and special projects as assigned Qualifications Required: - Degree in Statistics, Mathematics, Economics, Engineering, or any other quantitative streams with 2+ years of hands-on relevant analytics/data science experience - Minimum 2+ years of hands-on SQL/SAS programming experience & ability to leverage algorithms like Decision Tree, Regression - Experience with Business Intelligence and Reporting tools such as Tableau/Power BI - Experience in campaign performance measurement, customer targeting framework, and synergy of multiple functions - Strong communication skills to effectively lead analytics projects with senior stakeholders - Experience in the credit card or financial services industry Desired Skills/Knowledge: - Innovative mindset for improving capabilities and discovering new ones - Excellent SQL skills - Ability to manage multiple tasks with conflicting priorities As a Manager in the Analytics - H&W Platform role at Synchrony, you will play a crucial part in supporting the Health & Wellness platform business by providing strategic and scalable solutions, collaborating with functional teams, delivering high-impact projects, and working closely with analytics teams. Your role will involve hands-on problem-solving, delivering actionable insights, and ensuring effective decision-making through data analysis and automation of critical processes. Your expertise in analytics/data science tools, BI and reporting tools, and communication skills will be key in driving business growth and success.,

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 Safety (ISS) and Integrated Summary of Efficacy (ISE) reports. - Ensure accuracy and consistency across clinical studies and integrated data. - Develop, test, and implement reusable standard programs and SAS macros to automate routine tasks. - Prepare reviewer guides, data definition documents, and other materials for regulatory filings. - Collaborate with cross-functional teams including Statisticians, Clinical Data Management, Medical Writing, Regulatory, and Clinical Operations. - Accurately estimate programming efforts and ensure timely project delivery. Qualification Required: - Strong proficiency in SAS programming with experience in R preferred. - In-depth knowledge of CDISC standards (ADaM, SDTM). - Experience with regulatory submissions (FDA, EMA) and the clinical study lifecycle. - Knowledge of therapeutic areas such as Oncology, Immunology, Neuroscience. - Strong communication and leadership skills to guide teams and manage stakeholders. - Ability to handle multiple priorities and deliver high-quality results under deadlines.,

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 cleaning functions in order to maintain a clean data set. - Adherence to all written and authorized SOPs and/or work instructions. - Understand data structures, e.g, CDISC, LOINC - Experience of SAS programming to produce derived analysis datasets. - Collaborate with internal departments to make sure data is collected, managed and reported clearly, accurately and securely. - Support client and internal audits. - Takes on mentoring newer Data Management team members.

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 approved data cleaning functions in order to maintain a clean data set. - Adherence to all written and authorized SOPs and/or work instructions. - Understand data structures, e.g, CDISC, LOINC - Experience of SAS programming to produce derived analysis datasets. - Collaborate with internal departments to make sure data is collected, managed and reported clearly, accurately and securely. - Support client and internal audits. - Takes on mentoring newer Data Management team members. Location - Bangalore,Cochin,Kochi, Hyderabad,Karnataka,Kerala,Telangana

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 skills - Generating complex ad-hoc reports - Preparing and validating submission packages - Applying strong understanding/experience in Efficacy analysis - Taking on lead duties when required - Being a team player, willing to go the extra mile to achieve results and meet deadlines - Demonstrating adaptability and flexibility when priorities shift To be successful in this position, you should have: - At least 4+ years of statistical programming experience in the clinical development environment - A BA/BSc or higher degree in Statistics, Mathematics, Computer Science, Life Sciences, or a related scientific field - Proficiency in SAS data manipulation, analysis, and reporting - Familiarity with the drug development life cycle and experience in handling clinical trials data - Ability to work effectively in a globally dispersed team with cross-cultural partners - Strong oral and written English communication skills - Capability to deliver quality output within challenging timelines - Willingness to learn and adhere to company processes and procedures - Proficiency in complex statistical programming tasks - Ability to provide guidance to team members on technical and process questions Preferred qualifications include: - In-depth knowledge of SAS Graph and other SAS Statistical packages - Previous experience in publication work At Cytel, we prioritize our employees" success by offering consistent training, development, and support to ensure you thrive in your role.,

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 Figures (TFLs) covering safety and efficacy endpoints - Experience in programming patient narratives is considered a strong asset - Prepare Integrated Summary of Safety (ISS) and Integrated Summary of Efficacy (ISE) for submission packages - Conduct Pharmacokinetics (PK) and Pharmacodynamics (PD) data analysis, including non-compartmental analysis and support for modeling activities - Preferred experience in Oncology, Neuroscience, and Immunology studies Qualifications Required: - 3-4.5 years of experience in statistical programming - Technical expertise in SAS Programming, ADaM Dataset Development, TFL Generation, and PK/PD Analysis - Background in Therapeutic Area Expertise with experience in Oncology, Neuroscience, and Immunology studies (Note: The job description may not be exhaustive and additional tasks, duties, and responsibilities may be assigned at the company's discretion. Equivalent experience, skills, and education will also be considered for the role.),

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 areas to model the outcome of potential business strategies will also be part of your responsibilities. Qualifications: - Bachelor's Degree preferred; Associate's degree required. - Bachelor's Degree plus 4-6 years of analytics, consulting, project management, or equivalent experience preferred. - Advanced knowledge of job area typically obtained through advanced education and work experience. - Experience in managing projects/processes and working independently with limited supervision. - Ability to coach and review the work of lower-level professionals. - Familiarity with dedicated business intelligence applications and/or cloud services such as Domo, Looker, PowerBI, Qlik, Tableau, SiSense, as well as reporting capabilities of ERP, CRM, and database software vendors such as Oracle BI, Salesforce, SAP Business Objects, Pentaho, SSRS. Additional Information: - Proficiency in Power BI, SQL, and familiarity with Python and SAS Programming would be beneficial for this role.,

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 written and authorized SOPs and/or work instructions. - Understand data structures, e.g, CDISC, LOINC - Experience of SAS programming to produce derived analysis datasets. - Collaborate with internal departments to make sure data is collected, managed and reported clearly, accurately and securely. - Support client and internal audits. - Takes on mentoring newer Data Management team members.

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, collaborating with biostatisticians, and ensuring compliance with regulatory standards. What You Will Be Doing: Developing and validating SAS programs for statistical analysis and reporting of clinical trial data. Collaborating with biostatisticians to define analysis plans and statistical methods to be applied to clinical data. Performing quality control checks on statistical outputs and ensuring accuracy and consistency in reporting. Assisting in the preparation of statistical reports, presentations, and publications for regulatory submissions. Contributing to process improvements by identifying efficiencies in programming practices and methodologies. Your Profile: Bachelor s or Master s degree in Statistics, Mathematics, Computer Science, or a related field. Experience in statistical programming, preferably in a clinical research or pharmaceutical setting. Strong proficiency in SAS programming, with a solid understanding of statistical concepts and methodologies. Excellent analytical and problem-solving skills, with a keen attention to detail. Strong communication skills, with the ability to work collaboratively in a team environment and effectively convey complex information. What ICON can offer you: Our success depends on the quality of our people. That s why we ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: Various annual leave entitlements A range of health insurance offerings to suit you and your family s needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family s well-being. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here . Interested in the role, but unsure if you meet all of the requirementsWe would encourage you to apply regardless there s every chance you re exactly what we re looking for here at ICON whether it is for this or other roles. Are you a current ICON EmployeePlease click here to apply

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, collaborating with biostatisticians, and ensuring compliance with regulatory standards. What You Will Be Doing: Developing and validating SAS programs for statistical analysis and reporting of clinical trial data. Collaborating with biostatisticians to define analysis plans and statistical methods to be applied to clinical data. Performing quality control checks on statistical outputs and ensuring accuracy and consistency in reporting. Assisting in the preparation of statistical reports, presentations, and publications for regulatory submissions. Contributing to process improvements by identifying efficiencies in programming practices and methodologies. Your Profile: Bachelor s or Master s degree in Statistics, Mathematics, Computer Science, or a related field. Experience in statistical programming, preferably in a clinical research or pharmaceutical setting. Strong proficiency in SAS programming, with a solid understanding of statistical concepts and methodologies. Excellent analytical and problem-solving skills, with a keen attention to detail. Strong communication skills, with the ability to work collaboratively in a team environment and effectively convey complex information. What ICON can offer you: Our success depends on the quality of our people. That s why we ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: Various annual leave entitlements A range of health insurance offerings to suit you and your family s needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family s well-being. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here . Interested in the role, but unsure if you meet all of the requirementsWe would encourage you to apply regardless there s every chance you re exactly what we re looking for here at ICON whether it is for this or other roles. Are you a current ICON EmployeePlease click here to apply

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. Desirable Skills and Experience: - Proficiency in SAS programming - Expertise in SDTM and ADaM datasets This position is based in Chennai, India, and requires a Graduate or Post Graduate with a degree in life sciences. The role falls under the managerial category within the Data Sciences department and is a full-time position.,

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 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 Cytel we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will have: Bachelor s degree in one of the following fields Statistics, Computer Science, Mathematics, etc. At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor s degree or equivalent. At least 6 years of related experience with a master s degree or above. Study lead experience, preferably juggling multiple projects simultaneously preferred. Strong SAS data manipulation, analysis and reporting skills. Solid experience implementing the latest CDISC SDTM / ADaM standards. Strong QC / validation skills. Good ad-hoc reporting skills. Proficiency in Efficacy analysis. Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials data. Submissions experience utilizing define.xml and other submission documents. Experience supporting immunology, respiratory or oncology studies would be a plus. Excellent analytical & troubleshooting skills. Ability to provide quality output and deliverables, in adherence with challenging timelines. Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners. How you will contribute: Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs) Production and QC / validation programming Generating complex ad-hoc reports utilizing raw data Applying strong understanding/experience of Efficacy analysis Creating and reviewing submission documents and eCRTs Communicating with and/or responding to internal cross-functional teams and client for project specifications, status, issues or inquiries Performing lead duties when called upon Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc. Being adaptable and flexible when priorities change

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 Cytel we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will have: Bachelor s degree in one of the following fields Statistics, Computer Science, Mathematics, etc. At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor s degree or equivalent. At least 6 years of related experience with a master s degree or above. Study lead experience, preferably juggling multiple projects simultaneously preferred. Strong SAS data manipulation, analysis and reporting skills. Solid experience implementing the latest CDISC SDTM / ADaM standards. Strong QC / validation skills. Good ad-hoc reporting skills. Proficiency in Efficacy analysis. Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials data. Submissions experience utilizing define.xml and other submission documents. Experience supporting immunology, respiratory or oncology studies would be a plus. Excellent analytical & troubleshooting skills. Ability to provide quality output and deliverables, in adherence with challenging timelines. Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners. How you will contribute: Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs) Production and QC / validation programming Generating complex ad-hoc reports utilizing raw data Applying strong understanding/experience of Efficacy analysis Creating and reviewing submission documents and eCRTs Communicating with and/or responding to internal cross-functional teams and client for project specifications, status, issues or inquiries Performing lead duties when called upon Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc. Being adaptable and flexible when priorities change

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 study design and result evaluation. Utilize statistical software (e.g., SAS, R, JMP, or Python) to conduct data analysis, visualization, and reporting. Validate and verify data integrity, ensuring compliance with regulatory guidelines (FDA, ICH, GLP). Develop and review statistical analysis plans (SAPs), study protocols, and technical reports. Support regulatory submissions by preparing statistical documentation and reports. Stay updated with the latest statistical methods and best practices in in vitro research. Required Qualifications & Skills: Masters or Ph.D. in Statistics, Biostatistics, Bioinformatics, or a related field. 5 - 10 years of experience in statistical analysis of in vitro studies, preferably in the pharmaceutical, biotechnology, or life sciences sector. Strong knowledge of experimental design, regression models, ANOVA, DOE, and multivariate analysis. Proficiency in statistical software (SAS, R, JMP, Python, or equivalent). Experience with data visualization, trend analysis, and predictive modeling. Understanding of regulatory requirements and compliance standards (FDA, ICH, GLP). Excellent communication skills to present findings to cross-functional teams. Strong problem-solving skills and attention to detail. Preferred Qualifications: Experience in bioassays, pharmacokinetics, biomarker analysis, or toxicology studies. Familiarity with machine learning and AI-based statistical modeling. Knowledge of clinical and preclinical statistical applications.

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 proficiency in SAS and Python programming languages. Experience with data analysis and visualization tools. Excellent problem-solving skills and attention to detail. Ability to work collaboratively in a team environment. Strong communication and interpersonal skills. Familiarity with agile development methodologies. Minimum 6 years of experience in the IT Services & Consulting industry. Technical and Professional Requirements: SAS, Python, Base SAS Certified, Advanced SAS Certified Preferred Skills: Technology->sas->sas

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-driven recommendations to enhance business performance. WHATS IN IT FOR YOU? Accenture CFO & EV team under Data & AI team has comprehensive suite of capabilities in Risk, Fraud, Financial crime, and Finance. Within risk realm, our focus revolves around the model development, model validation, and auditing of models. Additionally, our work extends to ongoing performance evaluation, vigilant monitoring, meticulous governance, and thorough documentation of models. Get to work with top financial clients globally Access resources enabling you to utilize cutting-edge technologies, fostering innovation with the worlds most recognizable companies. Accenture will continually invest in your learning and growth and will support you in expanding your knowledge. Youll be part of a diverse and vibrant team collaborating with talented individuals from various backgrounds and disciplines continually pushing the boundaries of business capabilities, fostering an environment of innovation. What you would do in this role Engagement Execution Lead client engagements that may involve model development, validation, governance, strategy, transformation, implementation and end-to-end delivery of fraud analytics/management solutions for Accentures clients. Advise clients on a wide range of Fraud Management/ Analytics initiatives. Projects may involve Fraud Management advisory work for CXOs, etc. to achieve a variety of business and operational outcomes. Develop and frame Proof of Concept for key clients, where applicable Practice Enablement Mentor, groom and counsel analysts and consultants. Support development of the Practice by driving innovations, initiatives. Develop thought capital and disseminate information around current and emerging trends in Fraud Analytics and Management Support efforts of sales team to identify and win potential opportunities by assisting with RFPs, RFI. Assist in designing POVs, GTM collateral. Travel:Willingness to travel up to 40% of the time Professional Development Skills: Project Dependent Professional & Technical Skills: - Relevant experience in the required domain. - Strong analytical, problem-solving, and communication skills. - Ability to work in a fast-paced, dynamic environment. Advanced skills in development and validation of fraud analytics models, strategies, visualizations. Understanding of new/ evolving methodologies/tools/technologies in the Fraud management space. Expertise in one or more domain/industry including regulations, frameworks etc. Experience in building models using AI/ML methodologies Modeling:Experience in one or more of analytical tools such as SAS, R, Python, SQL, etc. Knowledge of data processes, ETL and tools/ vendor products such as VISA AA, FICO Falcon, EWS, RSA, IBM Trusteer, SAS AML, Quantexa, Ripjar, Actimize etc. Proven experience in one of data engineering, data governance, data science roles Experience in Generative AI or Central / Supervisory banking is a plus. Strong conceptual knowledge and practical experience in the Development, Validation and Deployment of ML/AL models Hands-on programming experience with any of the analytics tools and visualization tools (Python, R, PySpark, SAS, SQL, PowerBI/ Tableau) Knowledge of big data, ML ops and cloud platforms (Azure/GCP/AWS) Strong written and oral communication skills Project management skills and the ability to manage multiple tasks concurrently Strong delivery experience of short and long term analytics projects Additional Information: - Opportunity to work on innovative projects. - Career growth and leadership exposure. About Our Company | Accenture Qualification Experience: 10-12Years Educational Qualification: Any Degree

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 pharmaceutical and biotechnology clients. 1.5. Implement analyses specified in the protocol or the Statistical Analysis Plan (SAP) while working with the project statistician. 1.6. Ensure CRF meets the guidelines of the protocol and check for consistency and adequacy. 1.7. Write SAS programs to generate tables, listings, and figures and analysis datasets. 1.8. Review CRF annotations and data specifications. 1.9. Work in tandem with Biostatistics and Data Management member on various clinical projects. 1.10. Identify and edit checks per the data validation plan or data management plan. 1.11. Study management reports using SAS. 1.12. Validate the programmed analysis datasets, tables, listing and figures. 1.13. Perform analyses defined in the statistical analysis. 1.14. Prepare clinical and statistical summary reports. 1.15. Communicate with programming and statistics leads. 1.16. Utilize SAS programming skills within protocol team and perform all programming required for clinical trial analysis and reporting. 1.17. Perform quality control on final reports. 1.18. Develop SAS coding and table templates for preparing, processing and analyzing clinical data. 1.19. Establish monitoring of data transfers for ongoing trials to identify study conduct or data quality issues. 1.20. Provide input as required at all meetings, discussions and activities covering aspects of Statistical Reporting on project level activities. 1.21. As required, make certain that documents and specifications are consistent and comply with company standards for specifications of analysis datasets, listings, summaries, figures and tables for the clinical project 1.22. Program, according to specifications, analysis datasets, listings, tables, and figures for clinical projects and/or apply standard statistical methods to standardized PK study designs 1.23. Track milestones for project deliverables. 1.24. Maintain records for all assigned deliverables including archiving of project analysis and associated documentation. 1.25. Comply with pre-defined project / study standards and specifications. 1.26. Validate the programmed analysis datasets, tables, listing and figures. Utilize SAS programming skills within protocol team and perform all programming required for clinical trial analysis and reporting. 1.27. Develop SAS coding and table templates for preparing, processing and analysing clinical data. 1.28. Begins to develop a working knowledge of drug development and approval process 1.29. Other duties as assigned by reporting head or management Perks and Benefits Best in industry

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 according to the statistical analysis plan and other specifications. This includes working on SDTM, ADaM, or other derived datasets, tables, listings, figures, and reviewing case report form design. Additionally, you will need to follow Standard Operating Procedures (SOPs) and have a strong understanding of departmental and company procedures to guide others effectively. The ideal candidate for this position should have a degree in Statistics, Computer Science, or a closely related field. However, work experience may be substituted for the degree. You should have a minimum of 2 years of direct SAS programming experience in pharmaceutical development or CRO environment, along with good knowledge of medical terminology and the conduct and analysis of clinical trials. Knowledge of relevant industry data standards such as CDISC SDTM, ADaM, etc., is also required. Excellent oral and written communication skills, organizational skills, and attention to detail are essential for this role. At Advanced Clinical, we are committed to diversity and inclusion throughout our organization. We believe that a diverse staff enables us to draw on different perspectives, enhance our efficiency and effectiveness, and strengthen our legitimacy and relevance in delivering services to our clients. We value individuals from various backgrounds and cultures and prioritize an inclusive workplace that welcomes diverse ideas and appreciates valuable experiences. Advanced Clinical is an equal opportunity employer, and our commitment to diversity and inclusion applies to all aspects of employment. We provide accommodations for individuals with disabilities or handicaps to ensure a supportive and inclusive work environment. If you require any accommodations, please inform your Recruiter to discuss available alternatives.,

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-functional project teams. The Senior Statistical Programmer will mentor Statistical Programmers and external consulting resources. They must demonstrate a strong ability to integrate statistical concepts with SAS Programming efficiently and effectively and be able to work independently. Support development of technical programming specifications for SDTM, ADS, or ADaM standards. Independently develop and/or validate programs that generate SDTM and analysis datasets based on Alexion or ADaM specifications. Support development and validate technical programming specifications for tables, listings, figures/graphs based on Protocol and SAP. Independently develop and validate programs that generate tables, listings, figures/graphs using Alexion specifications. Manage external vendors and contract programmers. Provide project progress updates of programming activities. Review, maintain, and approve protocol-specific documents as necessary. Provide guidance and mentoring to peer, junior-level Programmers, and contract staff. Support project leadership ensuring that department standards are implemented in all studies. Contribute ideas and thoughts towards the optimization of standard operating procedures. Lead team meetings when appropriate. Any other activities as required. Essential Skills/Experience Minimum of 6 years of statistical programming experience in the Pharmaceutical, Biotechnology, or Contract Research Industry. Proven ability to: Develop and validate technical specifications and programs for safety and efficacy analysis datasets, tables, listings, and figures/graphs. Independently and collaboratively resolve problems. Clearly communicate processes and standards with management and team members. High competence in using SAS/Base, SAS/Macro, SAS/STAT. Knowledge of SAS/Graph, and SAS/SQL. Knowledge and implementation of: SDTM and ADaM principles. Relational Databases. Good Clinical Practice principles. Good Programming Practice principles. 21CFR Part 11 Standards principles. Integrated Summary Safety/Efficacy Analyses. Safety data and Coding Dictionaries (MedDRA and WHODD). ICH eCTD format. When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. Thats why we work, on average, a minimum of three days per week from the office. But that doesnt mean were not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. Joining Alexion means embracing an opportunity where work isn t ordinary. We are a beacon in the global Biopharmaceutical landscape. Our closeness to patients brings us closer to our work and each other. Combined with our brave, pioneering spirit we are truly unique in R&D and healthcare. At Alexion, grow and innovate in a business with a rapidly expanding portfolio. Enjoy the entrepreneurial spirit and autonomy of a leading biotech. You ll join an energizing culture where people build connections to explore new ideas and learn. As an important member of our team, youll meet the needs of some of the most under-served patients in the world. You will be empowered with tailored development programs designed not just for skill enhancement but for fostering a deep understanding of our patients journeys. You re supported by exceptional leaders and peers ready to lift you in marketing, compliance, and beyond. Alexion is proud to be an Equal Employment Opportunity and Affirmative Action employer. We are committed to fostering a culture of belonging where every single person can belong because of their uniqueness. The Company will not make decisions about employment, training, compensation, promotion, and other terms and conditions of employment based on race, color, religion, creed or lack thereof, sex, sexual orientation, age, ancestry, national origin, ethnicity, citizenship status, marital status, pregnancy, (including childbirth, breastfeeding, or related medical conditions), parental status (including adoption or surrogacy), military status, protected veteran status, disability, medical condition, gender identity or expression, genetic information, mental illness or other characteristics protected by law. Alexion provides reasonable accommodations to meet the needs of candidates and employees. To begin an interactive dialogue with Alexion regarding an accommodation, please contact Similar Roles Similar Roles Be the first to receive job updates and news from Alexion