418 Statistical Programming Jobs - Page 10

As a Biostatistician at CPVIA, a clinical data analytics solutions company in Hyderabad, you will utilize your expertise in statistical programming and consulting to support pharmaceutical, biotechnology, and medical device companies. Your primary focus will be on accelerating drug development activities while maintaining high quality standards and cost efficiency through collaboration with a team of experienced professionals. With a minimum of 3 years of experience in the pharmaceutical industry, you will play a crucial role in providing internal statistical support by closely working with lab scientists, technicians, statisticians, and programmers. Your responsibilities will involve collab...

You have a postgraduate degree in Biostatistics and possess 5-8 years of experience, or an equivalent combination of education and experience required to effectively carry out the key responsibilities of the job. Your expertise includes leading statistical activities in clinical research, particularly in pharmaceutical research or CRO settings. You are proficient in one or more statistical software packages, with a preference for SAS, for conducting statistical analyses. In this role, you will provide biostatistical consultation to clients and colleagues, formulate statistical objectives, experimental designs, and statistical analyses for research projects. Your responsibilities also include...

Statistics & Data Corporation (SDC) is a specialized contract research organization (CRO) based in Arizona, offering top-tier clinical trial services to pharmaceutical, biologic, and medical device/diagnostic companies since 2005. SDC provides technology-enabled services to equip clients with the necessary clinical services expertise and technology for successful clinical trials. As a Statistical Programmer at SDC, your primary responsibility will be to provide statistical programming support for clinical trials. This includes generating and validating analysis datasets, tables, listings, and figures for clinical trials, creating SDTM mapping and datasets, and maintaining the infrastructure ...

As a Senior Data Scientist at Mondelz International, you will play a crucial role in supporting the business by deriving valuable insights from data and effectively communicating your findings to various stakeholders. Your primary responsibilities will involve analyzing data using mathematical, statistical, and machine learning techniques to create actionable insights that drive data-driven decision making within the organization. Your key contributions will include formulating hypotheses, testing them through statistical modeling, and identifying trends or patterns that can be used to develop custom models or prototypes. You will collaborate with cross-functional teams to implement these mo...

As an Associate Director, Statistical Programming at Syneos Health, you will be part of a leading biopharmaceutical solutions organization focused on accelerating customer success. Our company is dedicated to translating clinical, medical affairs, and commercial insights into tangible outcomes that address the modern market landscape. In our Clinical Development model, we prioritize putting the customer and patient at the core of our operations. We are committed to simplifying and streamlining our processes to enhance collaboration and make Syneos Health a preferred partner. Whether you are engaged in a Functional Service Provider partnership or a Full-Service environment, you will work alon...

Remote Work: Hybrid Overview: At Zebra, we are a community of innovators who come together to create new ways of working to make everyday life better. United by curiosity and care, we develop dynamic solutions that anticipate our customer s and partner s needs and solve their challenges. Being a part of Zebra Nation means being seen, heard, valued, and respected. Drawing from our diverse perspectives, we collaborate to deliver on our purpose. Here you are a part of a team pushing boundaries to redefine the work of tomorrow for organizations, their employees, and those they serve. You have opportunities to learn and lead at a forward-thinking company, defining your path to a fulfilling career...

Biostatistician II statistical analyses for clinical research studies as outlined in statistical analysis plans, including creating statistical graphics and verifying randomization codes. They prepare statistical sections of protocols, including sample size calculations, annotate shell data displays, and provide specifications for the structure, content, and algorithms of status and analysis datasets. They perform and oversee quality control (QC) of data displays with inferential statistics. Statisticians report to the Biostatistics Manager. QUALIFICATIONS FOR ESSENTIAL FUNCTIONS Develop, validate, and maintain SAS programs to create analysis datasets, tables, listings, and figures (TLFs) as...

Skill required: Data Scientist - Data Science Designation: I&F Decision Science Practitioner Specialist Qualifications: Any Graduation Years of Experience: Experienced About Accenture Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. Visit us at www.accenture.com What would you do You will be aligned with our Insights & Intelligence vertical...

As a Clinical Data Manager at Clinvigilant Research Pvt. Ltd., a company of GSC Group, located onsite in Ahmedabad, you will play a crucial role in managing and overseeing the data collected during clinical trials. With 3 to 6 years of experience in clinical data management or a related field, you will ensure the accuracy, integrity, and compliance of clinical trial data with regulations. Your primary responsibility will be to oversee the collection, management, and quality control of clinical trial data. Working closely with clinical research teams, statisticians, and regulatory authorities, you will ensure that data is accurately recorded, processed, and analyzed for clinical trials. Your ...

For over 30 years, Beghou Consulting has been a trusted adviser to life science firms. We combine our strategic consulting services with proprietary technology to develop custom, data-driven solutions that allow life sciences companies to take their commercial operations to new heights. We are dedicated to client service and offer a full suite of consulting and technology services, all rooted in advanced analytics, to enhance commercial operations and boost sales performance. This role offers an exciting opportunity to leverage healthcare data and advanced analytics to optimize pharmaceutical commercial engagement, driving strategic insights that enhance sales performance, marketing effectiv...

Senior Statistical Programmer II (DMC) - Office or Home - 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 stat...

Senior Statistical Programmer II (DMC) - Office or Home - India 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 biostati...

Moniepoint is Africas all-in-one financial ecosystem, empowering businesses and their customers with seamless payment, banking, credit, and management tools. In 2023, we processed $182 billion and are Nigeria s largest merchant acquirer. Your Opportunity and Mission We are looking for talented and passionate Data Scientist to join the Growth team. Data science and optimization are key drivers for Moniepoint s business growth and the Data Scientist joining will have the opportunity to build and own the most important models starting from our attribution and Marketing Mix Models Contribute the following areas: channel attribution modeling, mCAC per channel modeling, LTV prediction, Marketing M...

In this role you will be part of our Centre of Excellence team working specifically in SDTM therefore extensive experience and knowledge is required in this area. What you'll be doing: Develops SAS programs to generate listings, tables and figures as outlined by mock TLF shells Performs quality control (source code review, double-programming and log review) of SAS programs Develops SAS programs to generate CDISC and other analysis data sets as outlined by respective specifications Prepares specifications for CDISC and other analysis data sets Assists Data Management with SAS programming needs Acts as Lead Biostatistical Programmer to interact with the Lead Biostatistician and the study team ...

The role of an SAS Developer at XpertDox in Noida, India involves developing and maintaining SAS programs, conducting statistical analyses, managing data, and ensuring the accuracy and efficiency of programs. As an SAS Developer, you will collaborate with cross-functional teams to enhance data-driven decision-making processes and improve healthcare outcomes. To excel in this role, you should have proficiency in Statistical Programming and general Programming skills. Strong Analytical Skills and knowledge of Statistics are essential for conducting effective statistical analyses. Experience in Data Management and data-driven decision-making will be beneficial in managing data efficiently. Your...

As a Data Scientist (AI & Machine Learning) at Infosys Finacle, located in Bangalore/Chennai, you will have the opportunity to be a part of transforming banking technology through the power of AI and data science. You will collaborate with top industry leaders to work on cutting-edge AI solutions, propose innovative ideas, and adapt in a fast-paced learning environment. Your responsibilities will include building AI algorithms, designing experiments to extract insights from large datasets, using predictive modeling to enhance customer experiences and achieve business goals, developing Explainable and Responsible AI models, conducting research to create prototypes, and identifying opportuniti...

Role & responsibilitie About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost o...

3- 8 years of experience for Sr Statistical programming position, having strong understanding of SAS Base/Macros/GTL and experience of SDTM/ADAM/TLFs creation as per CDISC standards. Expertise in Base and Advance SAS programming. Development of the complex SAS macros that can be utilized across TAs in multiple studies, review of the developed SAS programs. Expertise in SQL, SAS Macros, Functions, SAS GTL, SAS, and other advanced SAS components. Location : - Bengaluru,Mumbai,Pune,Hyderabad Contact Person : - Sangeetha Tamil

You have a postgraduate degree in Biostatistics and possess 5-8 years of experience, or an equivalent combination of education and experience to effectively carry out the key responsibilities of the job. You have experience in leading statistical activities in clinical research, particularly in pharmaceutical research or CRO settings. You are proficient in using statistical software packages, with a preference for SAS, to conduct statistical analyses for research projects. Your role involves providing biostatistical consultation to clients or colleagues, formulating statistical objectives and experimental designs, and conducting statistical analyses. You are responsible for providing advance...

As a Biostatistician at CPVIA, a clinical data analytics solutions company based in Hyderabad, you will play a crucial role in providing statistical programming outsource and statistical consulting services to pharmaceutical, biotechnology, and medical device companies. Your primary responsibility will be to offer internal statistical support by collaborating closely with lab scientists, technicians, and other statisticians/programmers within the team. Your expertise will be instrumental in supporting various drug development activities for our clients. To excel in this role, you must have a minimum of 3-10 years of experience in the pharmaceutical industry. A background in Sciences or Engin...

Summary -Responsible to support all statistical programming/data review reporting and analytics development aspects of assigned studies or project-level activities. About the Role Major accountabilities: 1. Produce and track reports for various line functions within Global Drug Development, used for ongoing monitoring of clinical data 2. Provide understandable and actionable reports on clinical data and monitoring of clinical data for key stakeholders 3. Facilitate interaction with end-user on creating specifications and working with programmers or performing the programming activities for successful delivery 4. To provide quantitative analytical support to the global program teams, includin...

As a Senior Clinical Data Analyst, you will be responsible for creating Data Management Plans (DMP), eCasebook Guidelines (eCCGs), Edit Check Specifications, Data Review Listing Specifications, and other set-up documents. You will also perform User Acceptance Testing (UAT) and review the Electronic Data Capture (EDC) database to ensure data consistency and completeness. Your duties will include Listings Review, Query Management, managing Serious Adverse Events (SAE) and external vendor data reconciliation, analyzing data trends, and generating reports. Additionally, you will be involved in User Account Management, Study Metrics, Quality Control (QC), and EDC Archival. In the role of Senior S...

Role & responsibilities Collaborates with field experts in Research and Pre-Clinical Development to plan, execute and analyze relevant experiments independently, notably design of experiments feasible under given lab conditions, support of sample-size calculations and application for animal testing licenses, randomization, data transfer into appropriate stats software, interpretation of results. Takes statistical responsibility for one or more standard experiments. Develops the statistical analysis plan for the experiments as appropriate, ensuring overall consistency within and between projects. Facilitates the overall organization and coordination of statistical activities for specific expe...

The Lead Biostatistician is a key member of the Department of Biostatistics & Programming, responsible for performing all Biostatistics tasks essential for clinical trial analysis and reporting. Collaborating closely with the Statistical Programming, Data Management, and Product Development departments, this position involves leading projects across studies or programs. As the primary contact with the sponsor for all biostatistics related activities on assigned projects, you will direct the activities of other biostatisticians to ensure timely completion of high-quality work. Your responsibilities include providing statistical support for clinical studies, developing and reviewing statistica...

Company Description CPVIA is a clinical data analytics solutions company based in Hyderabad (India) specializing in statistical programming outsource and statistical consulting services. Our experienced and expert team focuses on accelerating drug development activities across therapeutic areas with increased quality and optimum cost for pharmaceutical, biotechnology, and medical device companies. Role Description This is a full-time on-site role for a SeniorPrincipal Statistical Programmer at CPVIA in Hyderabad, with flexibility for remote work. The Principal Statistical Programmer will be responsible for statistical programming, data management, creating macros, and providing statistical e...