99 Adams Jobs

Finite Element Analysis (FEA/CAE) simulation capability using ABAQUS (preferred) and ANSYS. Simulation of Rubber parts , Metal brackets , and Plastic parts (advantageous). Basic knowledge of Rubber / Metal bracket / Plastic part design techniques. HyperMesh hex meshing of solid parts (basic level, added advantage). Basics of metal fatigue analysis (FE-Safe software exposure will be an added advantage) Actively contribute as a team player with an interest in long-term association Role & responsibilities. Design and Develop auto components and assemblies for automotive application. conduct simulations and analyze to validate design performance and reliability. Create detailed 3D Modules and en...

Primary Job Function Responsible for the integrity of the programming/computing solutions for multiple clinical trials (or equivalent) and/or publication activities. In collaboration with the Biostatistician and Senior Programmer, provide programming support to project-level programming deliverables and other adhoc programming requests. Roles and Responsibilities Ensure understanding and compliance with study and project programming standards. Responsible for development of programming specification. Create and Validate Safety and Efficacy Analysis Datasets in adherence with CDISC and client specific standards and maintain quality and accuracy. Create and Validate Safety and Efficacy Tables,...

Analyze and interpret complex clinical trial data using SAS.Develop and maintain databases, spreadsheets, and reports using Veeva.Collaborate with cross-functional teams to ensure accurate and timely delivery of results. Required Candidate profile Strong proficiency in SAS programming language.Experience with Veeva database management system.Excellent analytical and problem-solving skills.Ability to work independently and as part of a team.

Design, develop, and maintain complex statistical analysis systems using SAS.Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Required Candidate profile Strong knowledge of SAS programming language and its applications in clinical trial data management. Experience with SQL database management systems and querying languages.

Design, develop, and maintain complex statistical analysis systems using SAS.Collaborate with cross-functional teams to ensure timely delivery of high-quality results.Develop and implement efficient data processing Required Candidate profile Strong knowledge of SAS programming language and its applications in clinical trial data management. Experience with SQL programming language and database management systems.

Develop and maintain SAS programs for clinical trial data management, including data cleaning, transformation, and visualization.Collaborate with cross-functional teams to ensure timely delivery of high-quality deliverables. Required Candidate profile Strong knowledge of SAS programming language, including Base SAS, Enterprise Guide, and Macros. Experience with clinical trial data management systems, such as CDISC or Oracle Argus Safety.

Analyze and interpret complex clinical trial data to inform business decisions.Develop and maintain databases, spreadsheets, and reports using SAS and Veeva.Collaborate with cross-functional teams Required Candidate profile Strong proficiency in SAS programming language and Veeva software. Experience working with large datasets and performing complex data analysis tasks. Excellent problem-solving skills

Design, develop, and implement clinical trial data management systems using SAS.Develop and maintain databases for clinical trial data, ensuring data quality and integrity.Collaborate with cross-functional teams Required Candidate profile Strong knowledge of SAS programming language, including Base SAS and Enterprise Guide. Experience with clinical trial data management, statistical analysis, and database development.

Design, develop, and maintain complex statistical analysis systems using SAS.Collaborate with cross-functional teams to ensure timely delivery of high-quality results.Develop and implement data validation and quality control processes Required Candidate profile Strong knowledge of SAS programming language and its applications in clinical trial data management. Experience with SQL database management systems and data analysis tools.

Analyze and interpret complex clinical trial data to inform business decisions.Develop and maintain databases, spreadsheets, and reports using SAS and Veeva.Collaborate with cross-functional teams to design Required Candidate profile Strong knowledge of SAS programming language and Veeva software. Experience working with large datasets and performing complex data analysis tasks. Excellent problem-solving skills

Develop and maintain SAS programs for clinical trial data management, including data cleaning, transformation, and visualization. Collaborate with cross-functional teams to ensure timely delivery of high-quality deliverables. Required Candidate profile Strong knowledge of SAS programming language, including Base SAS, Enterprise Guide, and Macros. Experience with clinical trial data management systems, such as CDISC or Oracle Argus Safety.

Design, develop, and maintain SAS programs for clinical trial data management and analysis. Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Required Candidate profile Strong knowledge of SAS programming language and its application in clinical trial data management and analysis. Experience working with clinical trial databases and data management systems.

Design, develop, and maintain SAS programs for clinical trial data management and analysis. Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Required Candidate profile Experience working with clinical trial databases and data management systems. Excellent problem-solving skills and attention to detail.

Design, develop, and implement clinical trial data management systems using SAS. Collaborate with cross-functional teams to ensure seamless integration of clinical data into the development process. Required Candidate profile Develop and maintain complex statistical analysis plans and reports using SQL. Troubleshoot and resolve technical issues related to clinical trial data management.

Design, develop, and implement clinical trial data management systems using SAS.Collaborate with cross-functional teams to ensure accurate and timely delivery of project resultsDevelop and maintain complex databases using SQL Required Candidate profile Strong knowledge of clinical trial data management, statistical analysis, and database development. Proficiency in SAS programming language and SQL. Experience working with large datasets

Design, develop, and implement clinical trial data management systems using CDMS expertise. Collaborate with cross-functional teams to ensure seamless integration of clinical data into the overall study design. Required Candidate profile Strong understanding of clinical trial data management principles and practices.Proficiency in CDMS & SAS programming languages.Exp. working with large datasets and complex statistical analysis plans.

Design, develop, and implement clinical trial data management systems using CDMS expertise. Collaborate with cross-functional teams to ensure seamless integration of clinical data into the overall study design. Required Candidate profile Strong understanding of clinical trial data management principles and regulations. Proficiency in CDMS and SAS programming languages with at least 2 years of experience.

Design, develop, and implement clinical SAS programs for data management and analysis. Develop and maintain complex SQL databases for data storage and retrieval. Required Candidate profile Strong expertise in CDMS, clinical SAS programming, and SQL database management. Experience working with large datasets and developing complex data models.

Analyze and interpret complex clinical trial data using SAS. Develop and maintain databases, data systems, and computer models for clinical trial management. Collaborate with cross-functional teams. Required Candidate profile Strong proficiency in SAS programming language. Experience with Veeva or similar clinical trial management systems. Excellent analytical, problem-solving, and communication skills.

Design, develop, and implement clinical trial data management systems using SAS. Collaborate with cross-functional teams to ensure seamless integration of clinical data into the development process. Required Candidate profile Strong proficiency in SAS programming language and its applications in clinical trial data management. Experience with SQL programming language and its applications in statistical analysis.

Design, develop, and maintain SAS programs for clinical trial data management and analysis. Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Develop and implement data validation and quality control Required Candidate profile Strong knowledge of SAS programming language and its applications in clinical trial data management and analysis. Experience working with clinical trial databases and data management systems.

Design, develop, and implement clinical trial data management systems using CDMS expertise. Collaborate with cross-functional teams to ensure seamless integration of clinical trial data into the overall study design. Required Candidate profile Strong understanding of clinical trial data management principles and CDMS expertise. Proficiency in SAS programming language with experience in developing complex statistical analysis plans.

Design, develop, and implement clinical SAS programs for data management and analysis. Develop and maintain complex SQL databases for data storage and retrieval. Collaborate with cross-functional teams to identify business requirements Required Candidate profile Strong proficiency in SAS programming language, including Base SAS, Enterprise Guide, and Macros. Experience with SQL database management systems, including design, development, and maintenance.

Design, develop, and maintain SAS programs for clinical trial data management and analysis. Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Develop and implement data validation Required Candidate profile Strong knowledge of SAS programming language and its application in clinical trial data management and analysis. Experience working with clinical trial databases and data management systems.

As a Team Member in the engineering department, your role involves understanding the impact of various vehicle dynamic parameters such as RHB, NVH, Drivability, crash, etc. and maintaining a balance between cost, weight, and efficiency. You will need to have a good grasp of terminologies related to fuel efficiency and emissions, and be able to estimate the impact of changing vehicle parameters on emissions. Your responsibilities also include collaborating with testing teams, correlating CAE results with physical testing outcomes, and enhancing CAE models based on the analysis. Key Responsibilities: - Understand and analyze vehicle dynamic parameters for optimal performance - Estimate the imp...