Senior Principal Statistical Programmer Merck Group

9.0 - 13.0 years

0 Lacs

hyderabad, telangana

On-site

Role Overview: You will be joining as a Senior Principal Statistical Programmer, where you will have the opportunity to work with advanced technical solutions such as R, Shiny, and SAS. You will lead asset teams and mentor junior staff effectively, contributing to global assets across various therapeutic areas and shaping strategic decisions in statistical programming. Key Responsibilities: - Lead the trial or asset programming team as the Lead Statistical Programmer, ensuring that asset and trial delivery aligns with established timelines and quality standards. - Perform programming activities at both trial and asset levels, including the development of SDTM and ADaM datasets and the creati...

Posted 2 weeks ago

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Senior Product Analyst Saama Technologies Inc

1.0 - 5.0 years

0 Lacs

chennai, tamil nadu

On-site

As an Implementation Consultant reporting to the Product Owner, your key responsibilities will include creating User Requirement Specifications (URS) and functional requirement specs in Clinical Reporting and Analytics. You will be tasked with developing wireframes and mock-ups for clinical reports, as well as communicating with Clinical Data Management & Medical Reviewers to document clinical reporting needs. It is essential that you stay up-to-date with all Saama product features and releases. Your role will involve analyzing and understanding current business processes, events, and flows in Clinical Trial Development. You will act as a Clinical Subject Matter Expert, providing support for...

Posted 1 month ago

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Sr Statistical Programmer MEDTEK AI

4.0 - 8.0 years

0 Lacs

noida, uttar pradesh

On-site

As a qualified candidate for the position, you will be responsible for utilizing your strong SAS data manipulation, analysis, and reporting skills, along with a robust output programming experience. Your expertise in implementing the latest CDISC SDTM/ADaM standards will be essential for this role. Additionally, your familiarity with the drug development life cycle and experience in manipulating, analyzing, and reporting clinical trials data will be crucial. Your primary responsibilities will include the development and execution of statistical analysis and reporting deliverables, such as safety and efficacy analysis datasets, tables, listings, and figures. You will also be expected to devel...

Posted 1 month ago

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