Experience: 6-10 years Location: PAN India Work Mode: Full-Time | Remote Key Requirements We are looking for candidates with strong hands-on experience in: End-to-End SAS Programming in Clinical Trials ADaM and TLF development Strong Oncology TA experience
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ACL Digital (An Alten Group Company) hiring for Principal Statistical Programmer Interested candidates can share their updated resume Experience: 8 years relevant into SAS Notice: Immediate/30 Days Work location-Remote-India The Principal Statistical Programmer of Statistical Programming is responsible for
Role: Clinical Statistical Programmer Location : Hyderabad, Bengaluru, Pune, Chennai, Delhi NCR Mode of work : Onsite (5 days a week) Educational Qualification / Experience for the role: Masters degree with 6+ years of experience or bachelors
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: Create a requirements file detailing the functionality of a macro
Senior / Principal Statistical Programmer with Minimum (6 Months to 1 Year) of R programming. Experience Senior Statistical Programmer: 7+ years Principal Statistical Programmer: 9+ years Role Summary Responsible for end-to-end statistical programming activities for clinical studies, from specification
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 to
Job Responsibilities Uses SAS or other software to develop custom programming code to generate summary tables, data listings, graphs and derived datasets as specified in the statistical analysis plan and programming specifications. Works to ensure that outputs
RWE SAS Programmer Experience: 6–12 Years Location: Remote About the Role We are looking for an experienced SAS Programmer with a strong background in Real World Evidence (RWE) / Real World Data (RWD) to join our growing team. The ideal
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 to
Purpose: This function supports the protection of patient privacy when clinical trial data is shared externally. Typical use cases: Regulatory submissions Data sharing with researchers Health authority requests External collaborations Clinical trial transparency initiatives Typical responsibilities:
Senior Programmer I/II Purpose The role of the Senior Programmer I/II is to provide programming support to the statistics and programming department across a range of projects, clients and therapeutic areas. Key Responsibilities The job tasks listed below
Purpose: · Provide advanced technical expertise to develop and maintain programs/methodology to meet internal and external clientele needs. · Plan and lead the development of project-related solutions to the full scope of statistical programming tasks. ·
Role: Statistical Programmer Experience: 6–10+ years Locations: Remote Notice Period: Immediately to 15 days 1 . ADaM (Analysis Data Model) + TLF (Tables, Listings, and Figures) + R Programming 2. SDTM (Study Data Tabulation Model) + Metadata
Uses SAS, or other software, to develop custom programming code to generate summary tables, data listings, graphs and derived datasets as specified in the statistical analysis plan and programming specifications. Works to ensure that outputs meet quality
Job title : Assoc principal Stat Programmer - FSP Experience: 10+ Years Therapeutic Focus: Oncology / Immunology/Neuroscience Study Phase: Phase II & Phase III Location: PAN India Job Overview: We are seeking a highly experienced Senior/Lead Statistical