26 Adams Jobs

J OB DESCRIPTION Biostatistician II statistical analyses for clinical research studies as outlined in statistical analysis plans, including creating statistical graphics and verifying randomization codes. They prepare statistical sections of protocols, including sample size calculations, annotate shell data displays, and provide specifications for the structure, content, and algorithms of status and analysis datasets. They perform and oversee quality control (QC) of data displays with inferential statistics.Statisticians report to the Biostatistics Manager. QUALIFICATIONS FOR ESSENTIAL FUNCTIONS Develop, validate, and maintain SAS programs to create analysis datasets, tables, listings, and figures (TLFs) as specified in statistical analysis plans. Design and verify randomization codes to support clinical trial integrity. Prepare statistical sections of protocols, including sample size calculations, and annotate shell data displays. Provide specifications for the structure, content, and algorithms of status and analysis datasets. Perform and oversee quality control (QC) of data displays and analysis datasets to ensure accuracy and compliance with CDISC standards (SDTM, ADaM). Conduct independent validation of datasets created by other programmers or statisticians. Maintain project administration files, including protocols, annotated CRFs, statistical analysis plans, and programming/QC documentation. Manage electronic project directories to ensure organization and accessibility of deliverables. Mentor and guide junior programmers, providing training on SAS programming and clinical data standard EDUCATION AND EXPERIENCE REQUIRED Master's degree in Statistics or equivalent combination of Education and Experience (e.g. a Bachelors degree and at least 3 years of industry experience as a biostatistician) required A minimum of 3 years of experience as a statistician is required for the Senior Statistician position; a minimum of 1 year or EDETEK Training and supervisory approval is required for the non-Senior Statistician level Proficient in SAS and similar clinical data analysis software

As an Engineer/Senior Engineer in the Research & Development - Jaipur team at Hero Motocorp, your primary role as EDD- Engine Simulation will be to support HMCL in becoming a fast-growing company with increasing competence levels. You will be responsible for mechanical and fluid system design, development, and validation by understanding the fundamentals of design, development, and validation processes. Your expertise in optimizing CQT parameters will be crucial for the team's success. Your typical day will involve 1D and 3D simulation of various engine systems to gain a definitive understanding of their function and capability. This includes analyzing valvetrains, rotating and reciprocating systems, balancing systems, and selecting technology types to ensure reliability and durability. Additionally, you will be expected to utilize standardized toolsets such as GT-Suite, ABAQUS, ANSYS, ADAMS, AVL, and Ricardo for engine and transmission deliverables. To excel in this role, you should hold a B.Tech./M.Tech. degree and possess experience in 1D and 3D simulation of thermal and structural aspects in the 2W/4W industry. Your proficiency in modern toolsets like GT-Suite, ANSYS, ABAQUS, ADAMS, AVL, and Ricardo will be essential for delivering accurate simulation results. Apart from technical skills, behavioral attributes such as being a strong team player, willingness to share experience, openness to new ideas and technologies, and a dynamic work approach are highly valued in this role. Working at Hero Motocorp, the world's largest manufacturer of motorcycles and scooters, will provide you with the opportunity to collaborate with bright innovators dedicated to achieving excellence. As part of a brand that is celebrated by millions globally, you will contribute to shaping the future of mobility and innovation. If you are driven by ambitious dreams and unwavering determination, Hero Motocorp is the perfect place for you to thrive and grow professionally. Headquartered in New Delhi, Hero Motocorp is committed to developing modern, technologically advanced, and eco-friendly mobility solutions for its global customer base. With a strong presence in 47 countries, the company aims to achieve its next milestone of 100 million sales by 2030. Hero's focus on sustainability, innovation, and global expansion makes it a progressive and dynamic organization to be a part of. Join Hero Motocorp and embark on a journey of innovation, growth, and excellence in the automotive industry. Be a part of a legacy that is shaping the future of mobility and setting new benchmarks in the global market.,

Knowledge / Experience 4 to 6 years. Minimum 3 years in CAE preferably in commercial vehicles Essential: Experience in any CAE Pre-and Post-processor, reverent CAE tools. Experience in meshing for MBD models. Experience in model build and assembly for commercial vehicle parts. Theoretical knowledge of finite element analysis. Good communication, report writing, technical documentation and presentation skills. Qualification: BE/ B. Tech in Mechanical / Automobile Engineering from a recognized university. Role & responsibilities Preferred candidate profile

1. Design and development of CV, Steering and front axle aggregates 2. knowledge Bus and load platform 3. Casting and forging manufacturing processes knowledge, 4. DMEA, DFA, DFS, DFM. 5. Knowledge of DVP, 6 Hands on experience in CATIA. 6. Ability to resolve the problems, 7. Basic knowledge of vehicle dynamics ADAMs, MBD. 8. Knowledge of Homologation requirements.

Role & responsibilities Role : Mechanical Engineer Ananth Technologies pvt ltd is a three decade old establishment involved in the design and development of Aerospace, Defence and Satellite systems. Solar panels and associated mechanisms are a proven product line of Ananth which is attracted by both Indian and Overseas Space customers. We need a highly skilled and innovative Mechanical engineer with B.Tech/M.Tech with aptitude in Space sytem design,analysis, manufacture and manufacture Preferred candidate profile We need a highly skilled and innovative Mechanical engineer with B.Tech/M.Tech with aptitude in Space sytem design,analysis, manufacture and manufacture. The expertise shall include in the following satellite elements: 1. Honeycomb panels 2. Satellite mechanisms 3. Spring loaded Hinges 4. Hold down and Release mechanisms 5. Advanced materials including shape memory alloy The analytical abilities include; • Structural • Static and dynamic • Mobility • Thermal 3D CAD modeling on Solid works/UGNx etc Analysis on ANSYS/UGNx Mobility on ADAMS Experience on equivalent tools also would be considered

As a Senior Engineer specializing in Multibody Dynamics (MBD), your primary role will involve conducting vehicle level simulations using ADAMS-View/ADAMS-Car to assess and enhance performance parameters. Your responsibilities will also encompass performing MBD analysis at both sub-system and vehicle levels, including tasks such as building MBD models for KnC analysis, conducting Full vehicle Ride and Handling Simulations, as well as Load management simulations. Furthermore, you will be expected to utilize MBD analysis to assess design proposals, identify performance gaps and risks, and recommend design modifications to ensure compliance with specified requirements. Additionally, you will be responsible for optimizing performance through the use of analytical tools and collaborating with other stakeholders such as design, test, and CAE groups to provide project updates and drive performance enhancements. Overall, as a key member of the team, your expertise in MBD simulations and performance evaluation will be critical to the success of projects and the continuous improvement of vehicle performance.,

As a Team Member, you will be reporting functionally to the Group Lead/Team Lead and administratively to the Department Head. Your educational background should include a B.E/B.Tech/M.Tech degree in Mechanical/Automobile/Electrical Engineering. Having 5 to 7 years of experience in the field is essential for this role. Your responsibilities will include having a basic understanding of the chassis system, design aspects, and functions. You should also be familiar with part selection and the issues encountered during vehicle assembly. Experience with simulation software such as ADAMS, CARSIM, and Matlab is required. Additionally, you should possess knowledge of K&C simulation, ride and handling simulation, and tire modeling. Understanding vehicle dynamic parameters and terminologies related to ride, handling, and braking will be crucial for this role. You will need to estimate the impact of vehicle parameters on RHB and collaborate with testing teams to analyze failures. Interpreting results, identifying failure modes, and suggesting improvements for meeting performance criteria will be part of your responsibilities. In terms of competencies, you should have a thorough understanding of automotive engineering and regulatory guidelines and standards (e.g., SAE, JATMA, ETRTO, and AIS). Hands-on experience with chassis parts, knowledge in vehicle dynamics, ride handling, tire, and control systems, as well as familiarity with CAD software like UG NX, are required. Experience in project management will be an added advantage, and a minimum of 2 years of on-road driving experience is a must. From a behavioral standpoint, you should possess excellent interpersonal skills, effective communication and presentation skills, achievement orientation, teamwork abilities, and networking skills. Specific skills that are essential for this role include proficiency in MS Office, driving skills, and expertise in UG-NX, ADAMS, CARSIM, and Matlab.,

As a Senior Engineer in the field of Multibody Dynamics (MBD), your primary responsibility will involve conducting vehicle level simulations using ADAMS-view/ADAM-car to assess and enhance performance requirements. This will encompass various tasks such as building MBD models for KnC analysis, conducting full vehicle Ride and Handling simulations, and managing load simulations. Your role will also entail analyzing MBD data to assess design proposals, identify performance gaps and risks, and recommend design modifications to meet the specified requirements. Additionally, you will be expected to optimize performance using analytical tools and collaborate with other stakeholders including design, test, and CAE groups to provide project updates and enhance performance. Overall, your responsibilities will include project management aspects related to Vehicle level multibody dynamics (MBD) simulations to ensure performance requirements are met effectively and efficiently.,

Position: - Sales Engineer / Sr Sales Engineer- ESG Qualification: BE/ B Tech. in Electronics / Mechanical Experience: 2- 5 Years Location: Delhi /Hyderabad /Pune/ Kolkata The Sales Engineer is a customer facing role, responsible for the complete sales process - demand creation, mapping of accounts and closure. The candidate should be able to effectively communicate EDA / MCAD product capabilities and the benefits of the solutions through presentations and sales demonstrations. Conduct discovery and requirements gathering sessions to analyze and understand customer needs, workflows and technical requirements. Develop and/or collate sample documents, applications and other sales enablement materials for use during the sales and marketing sessions. Collaborate with Technical and services teams to specify, recommend and architect comprehensive customer solutions Required Skills : Relevant Sales experience in Defense / Institutional Sales /Private Commercial Sales/Academics Sales experience in Application or Engineering Software Knowledge on EDA tools Siemens EDA / Cadence / Synopsys Knowledge on MCAD tools Cero (ProE)/UGNX/Catia/Solid edge/Solid works/Inventor Knowledge on CAE Tools – Ansys/Nastran/Adams/Altair Knowledge of Procurement procedures such as Tender, Gem portal, E-tender, etc. Must be aware about the complete sales cycle Responsibilities: Identify customer needs and recommend suitable products/solutions Deliver product/concept presentations and conduct industry seminars Resolve client queries and manage sales concerns Capable of analyzing the merit of opportunities Skilled in identifying customer pain points Soft Skills: Team-oriented with strong analytical and presentation skills Creative, confident, and proactive Able to perform under pressure and meet targets Culturally adaptable with strong convincing skills Willing to travel extensively (70–75%) Role & responsibilities Preferred candidate profile

Role & responsibilities We are seeking a programming-skilled professional to join our Powertrain team. The ideal candidate should have strong expertise in software development, simulation tool integration, and automation to support our powertrain design and analysis processes. Domain Knowledge 1.Experience in SIL (Software-in-the-Loop) by integrating multiple simulation tools. 2.Skilled in co-simulation between tools such as Adams and MATLAB for seamless data exchange and enhanced model fidelity. 3.Proficient in MATLAB scripting (M-Scripting) and GUI development for automation and user-friendly interfaces. 4.Expertise in automating processes to improve efficiency and reduce manual effort. 5.Strong analytical and problem-solving abilities, enabling effective troubleshooting and optimization.

JD FOR R Programmer Title- Statistical Programmer/Sr. Statistical Programmer -R Programming We are seeking an experienced R Programmer to support Application development and statistical programming activities . The ideal candidate will have strong R programming skills with a solid understanding of clinical trial data, regulatory standards (e.g., CDISC, SDTM, ADaM), and open source libraries. Key Responsibilities: Develop and validate R programs to support CDISC dataset and statistical graph Create Markdown and Shiny appy for generating statistical tables and listings. Automate and streamline data wrangling, transformation, and visualization of clinical datasets using R and associated packages. Create and maintain Shiny apps, R Markdown reports, and automated pipelines for exploratory and statistical analyses. Collaborate with biostatisticians, data managers, and clinical teams to interpret clinical data and support study objectives. Contribute to statistical analysis plans (SAPs) and documentation for regulatory submissions (e.g., FDA, EMA). Ensure compliance with GxP, 21 CFR Part 11, and company SOPs in statistical programming deliverables. Required Qualifications: Bachelor's or Master's degree in Statistics, Biostatistics, Computer Science, Engineering or Quantitative field. 5+ years of experience in R programming within a clinical trials or pharmaceutical environment. Proficient in R packages such as tidyverse, haven, ggplot2, shiny, TEAL , knitr, and data.table. Knowledge of CDISC standards (SDTM, ADaM) and regulatory submission requirements. Experience with clinical data standards and regulatory documentation. Excellent attention to detail, problem-solving skills, and communication abilities. What We Offer: Opportunity to work on cutting-edge drug development programs. Career growth and access to global clinical research networks. Competitive salary and comprehensive benefits package.

MTech/ME in Mechanical (Thermal Engineering) 60% above in academics (10th, 12th, UG PG - No backlogs in any semester) Excellent English communication Good Presentation Skills Global internship/project experience in automotive industry is preferred for applications. Ready for 2 Year Trainee Agreement Ready for 2 Year Training agreement (Only if the training is scheduled in Germany for a designated period) Responsibility: Multibody simulation of commercial vehicle in Simpack Pre-processing, Simulation, Post processing ,result assessment ,validation corelation solution recommendation. Alignment with global colleagues for requirements and results. The candidate would need to interact and align with global group companies and external partners for development areas. The Trainee will support project tasks and learn various aspects of the product development process. Assist in project tasks, keeping the Team Leader / Team member / Cluster lead updated on progress and any arising issues adhering to quality. Prepare for and participate in technical reviews of assigned tasks. Enhance practical knowledge and experience in various processes and methods. Learn and understand organizational quality processes through agile methodologies. Requirements: Strong knowledge of multi body dynamics and vehicle dynamics Strong knowledge of linear flexible body generation FEM theroy Good know how of using CATIA V5 R 20 Basic hand on experience in any of one engineering simulation software like Simpack / Adams/ Hypeworks, Ansys / MATLAB for meshing, simulation post processing. Good understanding of virtual road load data acquisition Good knowledge of fundamental engineering principles and practices Good analytical skills, Knowhow in Automation languages Can able work in CFT to support to Project team. Knowledge of simulation scripting languages. Knowledge in PLM system

* Develop high fidelity full vehicle models using MSC ADAMS/Car * Perform Ride and Handling analysis using MSC ADAMS Car and interpret the results. * Should be able to perform static load generation analysis in ADAMS/Car and ADAMS/View environment. Required Candidate profile *Development of ADAMS/Car model and plausibility checking *Preparation and presentation of expressive reports as well as representation of ADAMS interests on project and customer level

Responsibilities Preparing MBD model for system level and vehicle level KC simulation, Ride and handling simulation, Tire modeling, Analysis of tire related market issues and co-simulation Results interpretation and report preparation Improve Virtual Testing for achieving better correlation with the Physical test Supporting design and testing team for vehicle performance improvements Experience of actual vehicle testing understanding of ride handling parameters with actual vehicle feeling as driver passenger is preferable Work closely with validation and testing teams to ensure alignment between virtual simulations and real-world testing activities Added advantage: ADAS Know-how Simulations using industry-standard tools and languages (e.g., CARSIM/MATLAB/Simulink, Python etc) Technical/Functional Bachelors/master s degree in mechanical, Automobile, Mechatronics Engineering Good Knowledge in area of Vehicle Dynamics, Ride handling, Tire, control systems Ability to perform virtual validation as per the physical testing conditions Ability to suggest countermeasure for design improvement and cost/weight reductions Ability to understand the market/prototype failures and capable to analysis the failures Candidate should have: Sound Knowledge of ADAMS, CARSIM Basic python, MATLAB Knowledge in in Model Based Development (MBD) ADAS area is preferable Behavioral Excellent interpersonal skills Communication presentation skills Achievement orientation Team player Networking skills

Role: Vehicle Strength Durability CAE Evaluation Responsibilities: CAE Modelling - Mesh discretization, Assembly, Constraint Load setting - for automotive sub-systems, primarily components related to Body Chassis Structure Closures. Carry out Strength Durability analysis - Linear Non-Linear cases. Interpretation of results, comprehending failure modes and providing directions for countermeasures for meeting performance criteria. Documentation of results and communication with stakeholders - design, testing - for implementation of failure countermeasures. Interact with Testing teams for analyzing failures, correlation of CAE results with physical testing results and making improvements in CAE model. Support in generation and evaluation of Value Enhancement proposals. Competency Requirements: Technical / Functional: Strong fundamentals in Strength of Materials, Machine design, Fatigue. Knowledge of Finite Element Analysis and related experience of working in Body Structures Closures CAE domain. Basic knowledge of Automotive Body Sheet metal design. Ability to prepare the CAE model in Hypermesh software, prepare input deck and perform analysis in Nastran LS-Dyna software, perform postprocessing in Hyperview LS Pre-Post. Working exposure in Fatigue evaluation - FEMFAT, MSC Fatigue, NCode- and Multibody software (like ADAMS) will be an added advantage. Basic exposure of Optimization softwares - Optistruct, Mode Frontier. Exposure to physical testing and ability to understand test conditions and its representation in CAE. Ability to suggest countermeasures for performance improvement.

Responsibilities: CAE Modelling - Mesh discretization, Assembly, Constraint Load setting - for automotive sub-systems, primarily components related to Body Chassis Structure Closures. Carry out Strength Durability analysis - Linear Non-Linear cases. Interpretation of results, comprehending failure modes and providing directions for countermeasures for meeting performance criteria. Documentation of results and communication with stakeholders - design, testing - for implementation of failure countermeasures. Interact with Testing teams for analyzing failures, correlation of CAE results with physical testing results and making improvements in CAE model Support in generation and evaluation of Value Enhancement proposals. Competency Requirements Technical / Functional : Strong fundamentals in Strength of Materials, Machine design, Fatigue. Knowledge of Finite Element Analysis and related experience of working in Body Structures Closures CAE domain. Basic knowledge of Automotive Body Sheet metal design. Ability to prepare the CAE model in Hypermesh software, prepare input deck and perform analysis in Nastran LS-Dyna software, perform post-processing in HyperView LS Pre-Post. Working exposure in Fatigue evaluation - FEMFAT, MSC Fatigue, NCode- and Multibody software (like ADAMS) will be an added advantage. Basic exposure of Optimization software's - Optistruct, Mode Frontier. Exposure to physical testing and ability to understand test conditions and its representation in CAE. Ability to suggest countermeasures for performance improvement. Behavioral: Excellent interpersonal skills, Communication presentation skills, Achievement orientation, Team player, Networking skills

Description Sr Stat Programmer (SDTM + ADAMs + TLF) Syneos Healthis a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities, Our Clinical Development model brings the customer and the patient to the center of everything that we do We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for, Whether you join us in a Functional Service Provider partnership or a Full-Service environment, youll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives, Discover what our 29,000 employees, across 110 countries already know: WORK HERE MATTERS EVERYWHERE Why Syneos Health We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program, We are committed to our Total Self culture where you can authentically be yourself Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people, We are continuously building the company we all want to work for and our customers want to work with WhyBecause when we bring together diversity of thoughts, backgrounds, cultures, and perspectives were able to create a place where everyone feels like they belong, 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 meet quality standards and project requirements, Performs validation programming and works with other programmers, biostatisticians, and other project team members to resolve discrepancies or any findings, Keeps project team members informed of programming progress and issues requiring their attention, Follow applicable SOPs, WIs, and relevant regulatory guidelines (e-g ICH), Maintains well organized, complete, and up-to-date project documentation, testing, and verification/quality control documents and programs ensuring inspection readiness, Manages scheduling and time constraints across multiple projects at a time, sets goals based on priorities from management, and adapts to timeline or priority changes by reorganizing daily workload, Develops specifications for datasets and outputs of any complexity according to statistical or sponsor requirements Anticipates and addresses potential programming issues, reflects forethought, establishes the basis for efficient programming and accurately definesall variables to be accepted by peer review and sponsor/requestor with little rework, Conducts effective internal meetings (appropriate in format, frequency and attendance) Distributes relevant information in advance Ensures minutes are promptly and accurately distributed Follows action items through to completion, and maintains order and focus of meetings, working toward consensus, Displays willingness to work with others and assist with projects and initiatives as necessary to meet the needs of the business, Accountable for on-time delivery across concurrent programming deliverables Negotiates programming timelines and provides risk mitigation plans for projects or programs, as needed Proactively informs management of the status of deliverables and significant project or program issues, including planned resolutions, Acts as the lead statistical programmer Directs the programming activities of other programming personnel and monitors progress on programmingdeliverables, Reviews project documentation such as Statistical Analysis Plan, mock shells, programming specifications, annotated CRFs, and SAS database design Provides feedback to the appropriate project team members which reflects forethought and reduces inefficiencies in programming activities, Participates in sponsor meetings, kickoff meetings, and bid defense meetings as statistical programming representative, as required by sponsor, Contributes to the mentoring of programming personnel through developing training courses, presenting training materials, reviewing work, and providing feedback or guiding new associates in process, Maintains a good working knowledge of clinical drug development, industry standards, and electronic submission requirements; serves as a technical expert resource to other department members for complex programming questions, Works cooperatively with other biostatistics and statistical programming personnel to establish standard operation procedures (SOPs), guidelines, policies, and/or procedures, Contributes technical expertise to the development of programming tools and macros for standardization and efficiency, When serving as a technical subject matter expert for CDISC and other industry and regulatory requirements, provides guidance and training to the Biostatistics group and other departments on the appropriate use of CDISC Standards When serving as a subject matter expert for CDISC and other industry and regulatory requirements, performs compliance reviews of project deliverables for CDISC deliverables including SDTM and ADaM specifications and datasets as well as any regulatory required documents (i-e DEFINE XML) When serving as a subject matter expert for CDISC and other industry and regulatory requirements, actively participates in industry standards organizations and provides regular updates to the Biometrics Department on upcoming changes to those standards, Transfers deliverables, Performs other work-related duties as assigned, Minimal travel may be required Qualifications Undergraduate degree, preferably in a scientific or statistical discipline; in lieu of degree, an equivalent combination of education and demonstrated programming experience, Extensive programming experience in SAS or other required software, preferably in a clinical trial environment as demonstrated by the ability to lead multiple complex and/or global projects with teams of statistical programmers, Knowledge and experience in the use of CDISC Standards for regulatory agency requirements Experience in submissions to a regulatory agency preferred, Experience in mentoring others in clinical trial process and CDISC Standards, Excellent written and verbal communication skills, Ability to read, write, speak and understand English, Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients, No matter what your role is, youll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment Learn more about Syneos Health, http://syneoshealth, Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above Further, nothing contained herein should be construed to create an employment contract Occasionally, required skills/experiences for jobs are expressed in brief terms Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job, Show more Show less

Location : Vijayawada , Andhra Pradesh Office timings : 1:30 Pm to 10 PM Client details : Channelsoft IT services Pvt Ltd Domain: Health Care (Clinical Trails) About Channelsoft Channel Soft is a pioneer in IT outsourcing and offshore software development business that envisioned and instigated the adoption of the flexible business practices that today enable our client companies to operate more efficiently and produce more value. Currently in India we have employees around 550+ working on various technologies like java,.net , DB, BI, AWS and support team . Office address : Nagarjuna nagar , near NTR university , Vijayawada . Responsibilities For Clinical SAS Programmer: Creating and executing SAS edit check programs Validating edit check programs using standard validation practices and processes Creating, validating and executing SAS programs and macros Utilizing SAS programming skills to provide ad-hoc reports (external and internal) and participating in project meetings (internal and external) Assist in developing programming specifications and in creating program specific validation plans Identifying and implementing solutions for complex reporting needs Creating and/or reviewing data editing and export specifications Working directly with clinical data manager and where needed with clinical project manager and other team members to ensure specifications are clear and accurate. Has a clear understanding of the contextual requirements for reporting outputs; and provides feedback Programming data cleaning/consistency checking programs to support internal applications for all therapeutic areas Programming and testing data export programs in accordance with specific client needs Documenting all programming and validation efforts in accordance with Good Clinical Practices Monitoring data integrity throughout a given study and utilizing SDTM guidelines to create transfer datasets Participating in the development of data editing conventions, specification documents and Clinical Data Management (CDM) processes Contributing to, designing and maintaining a library of reusable code Leading and managing enhancements to current CDM systems and providing inputs in the implementation of new systems Working independently and efficiently with minimal input required from the manager. Reviewing timelines; and projecting estimates and target dates in conjunction with direct supervisor and project team Adhering to target dates for project timelines and communicating any changes in target date to appropriate personnel including Project Manager Keeping department head informed of progress as well as potential impediments Adhering to established processes and standards Reading, understanding and adhering to organizational Standard Operating Procedures (SOP) Assisting in establishing and enforcing departmental standards Maintain and review clinical programming SOPs and participating in the modification of company SOPs Working with internal staff to resolve issues and exploring new opportunities to add value to organization and departmental processes Helping others to achieve results and performing other duties as assigned Attending and participating in applicable company-sponsored training Education: Bachelors or Masters degree in computer science, life sciences or related field preferred SAS Certified Professional considered a plus What were looking for 3 + years SAS programming experience in pharmaceutical related industry required (1 year with Masters degree) Experience working with CDISC, SQL and Relational Databases preferred Demonstrated programming skills required Working knowledge and solid understanding of database organization and how to extract data in order to generate listings and reports Proven ability in analyzing data and understanding of medical and/or clinical trial terminology is desirable Proven ability in problem solving and ability to work in group setting and independently; ability to adjust to changing priorities Excellent attention to detail and orientation toward meticulous work Strong interpersonal and communication skills, both verbal and written Strong documentation , organizational skills and ability to project and maintain a professional and positive attitude

Greetings from You & I Consulting! We've proudly helped candidates build careers at 64+ top MNCs across India, and were excited to bring you a new opportunity with a leading global company. If you have experience in Statistical Programming , this role is your next step forward! To Apply: Send your CV via WhatsApp or Call : Puja- (8250242229) or email your resume at :- puja@careersuni.com Shift - General Shift Open Locations :- Mumbai Pune Bangalore Hyderabad Indore Ahmedabad Key Responsibilities: Lead and oversee statistical programming activities for clinical trials at compound/indication/TA level Design and develop SDTM and ADaM datasets as per CDISC standards Generate Tables, Listings, and Figures (TFLs) for clinical study reports and regulatory submissions Manage and review deliverables for eSubmissions, including Define.xml and reviewer guides Provide technical leadership and mentorship to global programming teams Collaborate closely with biostatistics, data management, and regulatory affairs teams Support and lead Integrated Summary of Safety (ISS) and Integrated Summary of Efficacy (ISE) projects Ensure programming compliance with SOPs, FDA/EMA guidelines, and quality standards Required Qualifications: Bachelors or Masters degree in Statistics, Computer Science, or a related field 10+ years of SAS programming experience in clinical research or pharmaceutical industry Strong hands-on experience with ADaM, TFLs, eSubmissions, and integrated analysis Deep understanding of CDISC standards, regulatory compliance, and submission requirements Prior experience in oncology, neuroscience, or immunology domains preferred Proven leadership capabilities in managing cross-functional and global teams Excellent communication, project management, and problem-solving skills Preferred Tools & Skills: SAS (Base, Macro, STAT, Graph) Familiarity with SDTM/ADaM IG, FDA submission standards Understanding of regulatory submission formats (eCTD) How to Apply / Schedule an Interview: Send your details via WhatsApp or Call : Puja- (8250242229) in the following format: Full Name: Mobile Number: Email Address: Highest Qualification: Total Experience: Current Organization: Preferred Location: Current CTC: Expected CTC: Notice Period: Note: If the line is busy, please drop a WhatsApp message and we will get back to you at the earliest. Referrals Welcome! Know someone who fits the bill? Share this post and help them grow their career! You & I Consulting Your Career Growth Partner

TCS is hiring for Statistical Programmer!!! Job Location Mumbai/Pune/Bengaluru Experience Range 4 to 14 Years Educational Qualification(s) Required Any Life Science Graduate Interested can share their CV on babeeta.shahi@tcs.com Roles & Responsibilities:- Creation and validation of analysis data sets, tables, listings and figures . Creation and validation of ISS and ISE reports. . Development and testing of reusable Standard Programs . Development of SAS macros to work as utilities to automate routine activities . Remapping of old studies into ADaM structure . Build and maintain ADaM compliant Repository . Creation and validation of ADaM specification document . Assistance in creation of regulatory submission documents

Sales exp in Aerospace & Defense industry Knowledge on EDA tools Siemens EDA / Cadence / SynopsysKnow. on MCAD tools Cero(ProE)/UGNX/Catia/Solid edge/Solid works/InventorKnow on CAE Tools Ansys/Nastran/Adams/Altair

Sales exp in Aerospace & Defense industry Knowledge on EDA tools Siemens EDA / Cadence / SynopsysKnow. on MCAD tools Cero(ProE)/UGNX/Catia/Solid edge/Solid works/InventorKnow on CAE Tools Ansys/Nastran/Adams/Altair

Skill required: Life Sciences (AR&D) Services - SDTM Programming Designation: Business Advisory New Associate Qualifications: BE/BTech/Bachelor of Information systems and Management Years of Experience: 0 to 1 years What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the world's leading biopharma companies bring their vision to life enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.sdtm programmerProgram mapping of eCRF and external data into SDTM standards using SAS/ETL tools as applicable. What are we looking for? sdtm programmersdtm programmer Roles and Responsibilities: In this role you are required to solve routine problems, largely through precedent and referral to general guidelines Your primary interaction is within your own team and your direct supervisor In this role you will be given detailed instructions on all tasks The decisions that you make impact your own work and are closely supervised You will be an individual contributor as a part of a team with a predetermined, narrow scope of work Please note that this role may require you to work in rotational shifts Qualification BE,BTech,Bachelor of Information systems and Management

Hi We are looking to hire for SAS+R Programming. Please go through the JD and Apply Roles & Responsibilities: Create data cleaning reporting solutions, study status metric, and monitoring reports and visualizations required per standard and study specific data review plans. Contribute to process improvements and development of programming standards using R. Minimum of 3 years of experience in R programming including familiarity with R packages (e.g., Tidyverse, ggplot2, survival) Familiarity with data visualization techniques and tools in R. Write clean, efficient, and well-documented R code, conduct R code reviews, and R programming validation. Strong proficiency in R programming, including data manipulation, statistical analysis, and data visualization. Experience with POSIT Workbench, Connect, and/or Package Manager. Good to have python & SQL knowledge Develop library of reusable checks working closely with data engineers and config specialists. Collaborate with cross functional teams in creating business rules and automated check library across TAU. Serves as a technical resource for creating data analytics to help with data validation and cleaning. Provide programming expertise for data cleaning to efficiently ensure high quality data. Ensure accurate delivery by creating macros for Standard listings for the department based on specifications. Develop programs that generate CRF and Query metrics, including ad-hoc Sponsor and internal programming requests. Ability to set up and configure analytics for coding reports, safety review and any risk-based monitoring activities. Operational experience in pharmaceutical drug development with significant direct exposure to clinical development and data operations required for the reporting of clinical trial data (e.g. data review, regulatory submissions, safety updates, etc.) Understanding of regulatory requirements and relevant data standards; CDISC knowledge and experience are preferable. To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below: a) For Position in Bangalore Search : Job Code # 375 b) For Position in Hyderabad Search : Job Code # 376

Experience in clinical domain 6+ Years 1) Experience working on ADAM and TFL deliverables on multiple therapeutic areas and phases in clinical trials 2) Experience creating and working with Utility Macros 3) Experience creating specification 4) Experience with CDSIC standards including CDASH or SDTM/ADaM 5) Ability to work independently and as part of a team 6) Being open to new learnings and sharing with team members 7) Excellent communication skills [Written, Verbal, Interpersonal and organizational skills] 8) Proficient in using SAS EG/Studio for programming 9) Familiar with Unix environment and programming 10) Prior working experience in Vaccines or Oncology is an added advantage 11) Familiarity with multiple statistical procedures and functions to create TFLs Role & responsibilities Preferred candidate profile Perks and benefits