707 Sas Programming Jobs - Page 10

Core Purpose of the Role: To perform Biostatistical activities in Biometrics Department for Clinical Studies Phase 1-4 Role Accountabilities Reviewing protocol SAP & RAP preparation and implementation Sample size calculation Provides statistical consultations Preparing and reviewing randomization list Perform Statistical analysis as per SAP and Protocol Reviewing of SDTM and AdAM dataset Preparing and reviewing of tables, listing and graphs, as applicable Preparing and reviewing of statistical report, as applicable Provides support for blinding and unblinding documentations Preparing and reviewing standard operating procedures Training/Guiding/Mentoring associate biostatisticians and junior ...

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 ...

SUMMARY Job Title: SAS DI with Python Professionals Summary We are seeking highly skilled SAS with Python professionals to join our team. The ideal candidate will have a strong background in SAS programming, including SAS/BASE, SAS/SQL, SAS Macros, and relevant procedures. With a minimum of 6 years of experience and 5 years of relevant experience in SAS-Data Integrator with Python, the candidate will be responsible for designing, developing, and maintaining complex data integration solutions. The role requires strong analytical and problem-solving skills, as well as the ability to communicate technical information clearly to cross-functional teams. Location: Pune/Mumbai/Bangalore/Chennai Res...

As a Clinical Data Associate II at our company, your role involves providing data management support and assistance throughout the clinical trial data management process for assigned projects. You will follow Standard Operating Procedures (SOPs), regulatory directives, and study-specific plans. Your responsibilities include but are not limited to: - Supporting the Lead DM as a back-up or team member to ensure continuity and timely task completion - Performing data entry for paper-CRF studies when necessary - Conducting quality control of data entry - Developing CRF specifications from the clinical study protocol and coordinating feedback - Assisting in building clinical databases - Conductin...

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...

Proficiency in SAS programming (Base SAS, SAS/Macro, SAS/SQL, CAS actions) and Viya-specific tools (Visual Analytics, Model Manager, ESP for streaming). Hands-on with ML/AI: Building/deploying models using SAS Visual Data

Role Overview: As a Manager, Collections Strategy Delivery at Synchrony, your role is crucial in ensuring the validation of collections strategies or business rules to guarantee their proper implementation. You will work with various teams to validate pre-delinquent & delinquent processes, recovery/commercial processes, and alternate channel contact strategies. Your responsibilities will include developing actionable queries, creating exception & control reports, identifying process efficiency automations, and collaborating with stakeholders to streamline strategy requirements. Additionally, you will be involved in process improvement projects, conducting review calls, preparing detailed val...

The Principal Data Standards Analyst (Laboratory Expert) plays a crucial role in ensuring the accurate standardization, integration, and management of laboratory data across clinical studies. This role supports Clinical Information Governance (CIG), Trial Operations (TO) , Data integration, Translational Medicine, Sample Management, and external vendors, ensuring compliance with CDISC standards (SDTM, CDASH, Controlled Terminology) and regulatory requirements. The Principal Data Standards Analyst (Laboratory Expert) also provides specialized oversight on laboratory data handling, collaborating with internal teams and external central laboratories to mitigate risks related to biomarker, genom...

Purpose The role of the Principal Programmer is to provide programming support to the statistics and programming department across a range of projects, clients and therapeutic areas. The Principal Programmer may also perform a supervisory role (e.g. line management and/or project management). Key Responsibilities The job tasks listed below outline the scope of the position. The application of these tasks may vary, based on current business needs. Technical: Perform review of clinical trial documents including protocols, SAPs, CRFs, CSRs Author, review and approve study TFL shells and dataset specifications Author, validate and document SAS programs for datasets, TFLs and macros, applying goo...

Purpose The role of the Principal Programmer is to provide programming support to the statistics and programming department across a range of projects, clients and therapeutic areas. The Principal Programmer may also perform a supervisory role (e.g. line management and/or project management). Key Responsibilities Supporting with CDISC implementation of studies with Real world data QC of SDTM/ADaM datasets as required Review the aCRF, Specs, relevant documentation like SDRG/ADRG, Define.xml as relevant Expertise working across different disease areas like Oncology, Vaccines, Respiratory etc Guide Real World Programmers on NIS with CDISC expectations Technical: Perform review of clinical trial...

As a member of Risk Measurement team at one of the largest Buy side firm in the US, the candidate’s role will involve below- Conduct Risk Management by processing data for various asset classes from Custodians to third party risk analytics vendors. Partnering with IT and vendors to ensure accurate and complete data and risk analytics for Funds, Retail and Institutionally Managed accounts for around $700B of the $1 Trillion Assets Under Management/Advice Engaging with internal Risk SMEs and data operations team for resolving issues with source data, analysing and validating data and the end reports and fixing exceptions in both the daily and monthly risk process Managing data collection proce...

Manager, CSAR - SAS Edit Check Programmer What you will do The Manager, CSAR - SAS Edit Check Programmer will report to the Sr. Manager, Clinical System and Analytical reporting and will be focused on supporting SAS Edit check programming activities. The Manager, CSAR - SAS Edit Check Programmer will create and implement edit checks, adhering to Amgen standards, procedures, and best practices using SAS programming. The position is expected to partner effectively with other CSAR Operations and cross functional staff to seamlessly ensure high quality deliverables, internal and external clinical systems, and other CSAR activities related to the use electronic data capture technology. The positi...

What you will do Amgen is expanding its Global Statistical Programming (GSP) capabilities, with Amgen India (AIN) playing a key role in supporting integrated delivery across regions. As a Senior Manager of Biostatistical Programming (Programming Execution Lead), you will partner with the Global Programming Lead (GPL) and lead an offshore team of Study Lead Programmers (SLP) and Study Programmers (SP) to ensure successful execution of end-to-end programming activities for products within or across therapeutic areas. Together with the GPL, this Senior Manager will be accountable and responsible for Global Statistical Programming study results and drug approval submission activities for the ass...

What you will do The Associate Vice President, Clinical Data Management is a member of the Global Development Operations (GDO) leadership team and is a strategic partner to the R&D organization. The AVP will lead Amgens Clinical Data Management function within GDO, ensuring the highest quality of clinical data collection, processing, and analysis to support regulatory submissions and clinical development programs. This role is responsible for the strategic direction, leadership, and operational oversight of data management processes supporting clinical trials across all therapeutic areas and phases. This AVP will collaborate closely with cross-functional teams including clinical operations, ...

What you will do In this vital role you will be the Manager, CSAR - SAS Clinical Data Reporting and Spotfire Programmer will work with the Sr. Manager, Clinical System and Analytical reporting and will be focused on supporting SAS Clinical Data Reporting and Spotfire programming activities. The Manager, CSAR - SAS Clinical Data Reporting and Spotfire Programmer will create patient data reports and dashboards, adhering to Amgen standards, procedures, and best practices using SAS for programming and Spotfire for visualization. The position is expected to partner effectively with other CSAR Operations and multi-functional staff to seamlessly ensure high quality deliverables, internal and extern...

What you will do In this vital role you will be responsible for manipulating large databases and generating reports to partner with epidemiologists to explore and generate RWE from real-world healthcare data assets. The ideal candidate should possess a bachelors degree and have at least six years of relevant career experience in statistical programming. Proficiency in SQL programming and SAS or R programming is required. The successful candidate will demonstrate scientific and technical excellence, exceptional oral and written communication skills, problem-solving abilities, and meticulous attention to detail. The ability to work effectively within a large, globally distributed team is essen...

What you will do Amgen is expanding its global Statistical Programming capabilities, with Amgen India (AIN) playing a key role in supporting integrated delivery across regions. As Sr. Director of Statistical Programming, you will provide local functional leadership from AIN, supporting global clinical development programs in close partnership with global teams through seamless execution that leverages digital innovation to drive quality deliverables, operational excellence, and regulatory compliance. Responsibilities: Provide strategic and operational leadership for statistical programming delivery within Amgens global framework, with site accountability based in AIN. Oversee the execution o...

As a SAS Data Engineer, you will be responsible for the following: - Strong experience with SAS programming, including SAS/BASE (Data Step programming), SAS/SQL, SAS Macros, and relevant procedures (e.g., Proc SQL, Proc Transpose). - Familiarity with ETL processes, data warehousing concepts, and related tools. - Knowledge of data validation, data quality principles, and data lineage. - Ability to analyze business requirements, understand use cases, and contribute to design and architecture decisions. - Strong analytical and problem-solving skills to address complex data challenges and resolve user issues. - Ability to work effectively with cross-functional teams and communicate technical inf...

Position Overview: As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills to support one or more Phase I-IV clinical trials, with a focus on Oncology. To be successful in this position you will have: At least 5 years of relevant statistical programming experience in a clinical development environment with 3 years of efficacy preferred. BA/BSc or higher degree in Statistics, Mathematics, Computer Science, Life Sciences, or other related scientific subjects. Excellent SAS data manipulation, analysis, and reporting skills. Ability to implement the latest CDISC ADaM standards (production/validation). Strong understanding/experience with ADaM efficacy dataset d...

Position Overview: As a Senior Statistical Programmer, you will perform programming activities for the creation and validation of SDTM domains by implementing CDISC standards and working on pooled studies ADaM datasets for ISS and submission packages with a focus on Oncology. To be successful in this position you will have: At least 5 years of relevant statistical programming experience in a clinical development environment. BA/BSc or higher degree in Statistics, Mathematics, Computer Science, Life Sciences or other related scientific subjects. Demonstrates advanced experience with all SAS language, procedures, and options commonly used in clinical trial reporting including the Macro languag...

Ensures that the Statistical Programming department meets timelines, provides high quality deliverables, complies with contractual project requirements and Standard Operating Procedures (SOPs), and conducts projects within budget. • May participate in the development of department SOPs and guidelines, promoting standardized and consistent processes to maximize the efficiency of the Statistical Programming department. • Responsible for staff development, training and retention. Oversees development of direct reports by setting goals, managing performance, evaluating and monitoring training needs, supporting development plans, mentoring, and coaching. • Facilitates succession planning and main...

About The Role Project Role : Application Lead Project Role Description : Lead the effort to design, build and configure applications, acting as the primary point of contact. Must have skills : SAS Analytics Good to have skills : Agile Project Management, Data Engineering, PySpark Minimum 15 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Application Lead, you will lead the effort to design, build, and configure applications, acting as the primary point of contact. Your typical day will involve collaborating with various teams to ensure that application development aligns with business objectives, facilitating discussions to gather re...

As a Senior Statistical Programmer / Principal Statistical Programmer with 5+ to 12 years of experience in Bangalore, you will play a crucial role in developing specifications for SDTM datasets and SDTM datasets specifications for Clinical Data Analysis (CDA configuration) module in elluminate. Your primary skills should include SDTM, ADAM, TLF, CDISC, and Study lead experience. The key responsibilities of your role will involve developing SAS programming to produce SDTM datasets and SDTM datasets for CDA configuration, as well as developing specifications for Analysis Data Model (ADaM) datasets and SAS programming for ADaM datasets. Additionally, you will be responsible for developing and m...

Role Overview: As a Senior SAS Programmer at the rapidly growing corporate office in India, Mumbai, you will play a vital role in the Biostatistics team. Your primary responsibility will be to propose and develop specifications for new projects, lead project teams, and write SAS programs for creating analysis datasets, tables, listings, and figures. Your expertise in SAS programming and adherence to CDISC standards will be crucial for the success of projects. Key Responsibilities: - Propose and develop specifications for new projects and lead project teams - Write SAS programs for creating analysis datasets, tables, listings, and figures - Program, validate, and maintain mapped databases usi...

As a Senior Clinical Data Associate at [Company], you will be responsible for providing data management support and assistance throughout the clinical trial data management process. Your role will involve following Standard Operating Procedures (SOPs) and regulatory directives to ensure the successful completion of assigned projects. Some key responsibilities include: - Supporting the Lead DM as a back-up and/or team member to ensure tasks are performed in a timely manner - Performing data entry for paper-CRF studies and conducting quality control of data entry - Assisting in developing CRF specifications and coordinating the review/feedback from stakeholders - Building clinical databases an...