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10.0 - 14.0 years
0 Lacs
hyderabad, all india
On-site
As an Associate Director Statistical Programmer, you will have the opportunity to work with advanced technical solutions such as R, Shiny, and SAS, allowing you to lead asset teams and mentor staff effectively. In this role, you will contribute to global assets across a variety of therapeutic areas, shaping strategic decisions in statistical programming. - Lead one or more asset programming teams 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 creation of specifications. - Develop and v...
Posted 1 week ago
1.0 - 5.0 years
0 Lacs
chennai, all india
On-site
As an Implementation Consultant at our company, your role will involve the following key responsibilities: - Responsible for creating User Requirement Specifications (URS) and functional requirement specs in Clinical Reporting and Analytics. - Create wire-frames and mock-ups for Clinical reports. - Communicate with Clinical Data Management & Medical Reviewers to document the clinical reporting needs. - Stay up-to-date with all Saama product features and releases. - Analyze and understand current business processes, events, and flows in Clinical Trial Development. - Act as a Clinical Subject Matter Expert and provide Clinical Project Support. - Author and document business requirements, provi...
Posted 1 week ago
8.0 - 12.0 years
0 Lacs
noida, uttar pradesh
On-site
As a data science-driven company focused on supporting faster drug development and healthcare solutions, MEDTEK AI's team is comprised of senior statisticians, data scientists, statistical modeling and programming experts, data visualization specialists, cloud data engineers, data lake strategists, and regulatory submission and drug safety consultants. In this role at MEDTEK AI, you will be involved in a hands-on programming position, supporting deliverables in the study/project/portfolio/standards team, focusing on medium or high complex statistical programming deliverables. Your responsibilities will include: - Demonstrating strong SAS data manipulation, analysis, and reporting skills with...
Posted 1 month ago
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 months ago
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 2 months ago
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 3 months ago
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