Job Overview Conduct testing activities in CDMS environment and provide comprehensive testing expertise to the team to produce efficient, quality database that meets customer requirements. Essential Functions • Independently conduct testing activities to validate edit checks,
Key Responsibilities Develop, validate, and maintain ADaM datasets, TLFs, and other analytical outputs for clinical trials. Support Oncology studies by ensuring accuracy, consistency, and regulatory compliance in all programming deliverables. Contribute to ISS/ISE activities, including dataset integration,
Senior/ Principal Statistical Programmer (SAS & R) Location: Bangalore/Hyderabad/India Remote Opportunities Veramed prides itself on two key areas: providing the highest quality statistics and programming consultancy for its clients, and giving its employees an industry leading working environment
At EY, were all in to shape your future with confidence. Well help you succeed in a globally connected powerhouse of diverse teams and take your career wherever you want it to go. Join EY and
At EY, we’re all in to shape your future with confidence. We’ll help you succeed in a globally connected powerhouse of diverse teams and take your career wherever you want it to go. Join EY and
Job Title: Senior Statistical Programmer (Oncology) Location: Canada/IN Employment Type: Full-Time Experience: 8+ Overview We are seeking an experienced Senior Statistical Programmer with strong Oncology clinical trial experience to support end-to-end clinical programming activities. This role requires
Key Responsibilities Extract and analyze large volumes of transactional data from Amazon Redshift databases, including both header and detail-level transaction records for restaurant locations. Develop and maintain SAS programs to retrieve data for selected stores, products, pricing
R (Proficient)+SDTM (Proficient)+ADAM(Expert)+Efficacy(Proficient)+TLF(Expert)+Submissions(Proficient) Develop and validate SDTM and ADa M datasets as per CDISC standards Perform statistical programming using SAS and R Generate Tables, Listings, and Figures (TLFs) for clinical studies Conduct efficacy analysis to support study outcomes
Key Accountabilities: Create eCRF specifications, design, develop and unit test and functionally validate clinical trial setup process Create edit check specifications and program or modify checks at study level within EDC Setup different instances of study
Company Description HVES is a reputed engineering firm specializing in high-voltage electrical projects and solutions. Based in the Netherlands, the company is committed to delivering innovative, reliable, and sustainable energy solutions to a wide range of
Team Lead Site Service Location: Kochi, Nagpur Openings: 1 Position Overview The Team Lead – Site Services is a senior field leadership role responsible for end-to-end execution of industrial automation and control system projects at client
Job Responsibilities Works on issues of limited scope. Follows established practices and procedures in analyzing situations or data from which answers can be readily obtained. Work is reviewed upon completion and is consistent with departmental objectives.
Catalyst Clinical Research provides customizable solutions to the biopharmaceutical and biotechnology industries through Catalyst Oncology, a full-service oncology CRO, and multi-therapeutic global functional and CRO services through Catalyst Flex. The companys customer-centric flexible service model, innovative technology, expert
Nissan is a pioneer in Innovation and Technology. With a focus on Mobility, Operational Excellence, Value to our Customers and Electrification of vehicles, you can expect to be part of a very exciting journey here at
Job Overview Conduct testing activities in CDMS environment and provide comprehensive testing expertise to the team to produce efficient, quality database that meets customer requirements. Essential Functions • Independently conduct testing activities to validate edit checks,
Sponsor-dedicated: 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 Principal Statistical Programmer, you will be dedicated
Sponsor-dedicated: 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
Senior / Principal Statistical Programmer(s) with strong hands-on expertise in R (mandatory) and SAS , (Primary requirement: Programmer with strong SDTM expertise) Required: Strong SDTM expertise Oncology study experience Proficient in SAS and R Good working knowledge of
Job title: Senior/ Principal Statistical Programmer Location: Remote/Hybrid – Bangalore Veramed prides itself on two key areas: providing the highest quality statistics and programming consultancy for its clients and giving its employees an industry leading working environment
Job title : Senior Statistical Programmer - FSP Experience: 7 + Years relevant experience and hands-on R programming skills. Location: PAN India Job Overview Provide experienced technical expertise to develop process methodology for department to meet internal