HiHiring for the leading ITES Company for Regulatory Medical Writer Profile.Roles and Responsibilities:Prepare and review clinical documents that are part of regulatory submission including but not limited to Protocol, Clinical Study Pharmacology Report, Clinical Study Report, Narratives, and Post Approval Documents across the Therapeutic Areas. Quality check of the clinical documents that are part of regulatory submission including but not limited to Protocol, Clinical Study Pharmacology Report, Clinical Study Report, Narratives, Clinical Summary of Safety, Clinical Summary of Efficacy and Common Technical Document Modules. Initiate start up meetings with the Study Teams related to the creation and development of the clinical document for regulatory submission, if required. To work in coordination with all the members in the study team- internal and external for the development of clinical documents. Share project timelines amongst the study team for the development of document. Prepare Clinical Documents according to the Standard Operating Procedures, Document Standards and Guidance document. Review statistical analysis plans and table/figure/listing, when required. Ensure uniformity and consistency in the scientific content of the regulatory documents To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below:a) For Position in Mumbai Search : Medical Writing Mumbai (Job Code # 56)b) For Position in Pune Search : Medical Writing Pune (Job Code # 57)

HiWe are Hiring for the ITES Company for the position of SAS: Statistical ProgrammerJob Description: We are looking for an associate with at least 5 - 10 years of experience for Statistical programming position, having strong understanding of SAS Base/Macros/GTL and experience of SDTM/ADAM/TLFs creation as per CDISC standards. Associate should be able to manage communication with customers, track and ensure quality on-time deliverables, suggest and drive implementation of process improvements for enhanced quality and efficiency gains, institute robust processes to ensure consistent outcomes with quicker turn-around time.Expertise in Base and Advance SAS programming. Expertise in developing macros and developing generalized programs. Development of the complex SAS macros that can be utilized across TAs in multiple studies, review of the developed SAS programs.Expertise in SQL, architecting Data Preparation, Data Visualization, Data Integration, Analytical Reporting. Worked on different SAS tools like SAS Data Integration, SAS Studio, SAS EG, SAS Management Console. SAS Developer with over 5+ years of experience with expertise on different domains. Possess solid ability in integrating programming skills, adapting to new applications and expertise in architecting Data Preparation, Data Visualization, Data Integration, Analytical Reporting. Worked on different SAS tools like SAS Data Integration, SAS Studio, SAS EG, SAS Management Console. Experience in ETL Preparation, data exploration, data preparation, data cleansing, reporting, and technical document preparation. Import /Export data using various techniques like PROC IMPORT, PROC EXPORT, LIBNAME, INFILE, PROC PRINT statements. Good Knowledge of Data management, Data handling, and Creating Data structure Knowledge of Database languages such as MYSQL, Oracle. Knowledge of various SAS Procedures like PROC Means, PROC Freq, PROC Contents, PROC Import, PROC Format, Proc Summary, PROC Sort, PROC Transpose, and PROC Report. Knowledge Of SAS procedures like SAS/Base, SAS/Macro, SAS/SQL, SAS Arrays, Do loops, SQL Joins, Hash join techniques To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below:a) For Position in Mumbai Search : Statistical Programmer Mumbai (Job Code # 208)b) For Position in Pune Search : Statistical Programmer Pune (Job Code # 209)

HiWe are hiring for ITES Company for Spotfire Programmer Role.Responsibilities:Working on Refreshes requests for SRT & CSTVBuilding Oncology & Standard Visuals for Clinical Study Team Visualization (CSTV)Setting up standard and Study Specific requests for Safety Review Team (SRT)Knowledge of Spotfire, Study configuration tool and On Demand Tool.Creating SAS Codes as per the requirementValidation of visuals as per the specifications1.5+ years of experience crafting interactive dashboards using TIBCO Spotfire. Adept at developing complex reports utilizing cross tables, bar charts, with advanced features like: property control, custom expressions, labels, and marking. Proficient in all core visualizations including bar charts, line charts, pie charts, scatter plots, cross tabs, and combination charts. Experience creating intricate dashboards leveraging information links and Iron Python scripting for enhanced functionality. Possess strong knowledge of advanced visualizations such as heat maps, box plots, tree maps, and map charts. Proven ability to collaborate effectively with stakeholders to address support requests and implement new feature enhancements. Skilled in publishing and deploying dashboards to meet specific business requirements. Proficient in Microsoft Excel functions including VLOOKUP, text functions, charts, and pivot tables. Demonstrated ability to handle multiple tasks simultaneously and thrive in both independent and collaborative work environments. Possess strong documentation and presentation skills to effectively communicate technical concepts. To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below:a) For Position in Mumbai Search : Spotfire Programmer Mumbai (Job Code # 78)b) For Position in Pune Search : Spotfire Programmer Pune (Job Code # 79)

Hi, We are hiring for Leading ITES Company for SAS Programmer & CDB Programmer (J Reviewer/Python/SAS)Role & responsibilities:1.Create data cleaning reporting solutions study status metric, and monitoring reports and visualizations required per standard and study specific data review plans. 2. Develop library of reusable checks working closely with data engineers and config specialists.3. Collaborate with cross functional teams in creating business rules and automated checklibrary across TAU.4. Serves as a technical resource for creating data analytics to help with data validation and cleaning.5. Provide programming expertise for data cleaning to efficiently ensure high quality data. 6. Ensure accurate delivery by creating macros for Standard listings for the department based on specifications. 7. Develop programs that generate CRF and Query metrics, including ad-hoc Sponsor andinternal programming requests. 8. Ability to set up and configure analytics for coding reports, safety review and any risk-based monitoring activities.9. 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.) 10. Understanding of regulatory requirements and relevant data standards; CDISC knowledge and experience are preferable 11. Technical skills and experience using relational databases (e.g. MS SQL Server, Redshift, or Oracle),12. EDC build and/or clinical data management experience preferred 13. Experience in AWS preferred14. Experience setting up automated validation is preferred15. Knowledge of Data lake and creating interactive Dashboards are preferred16. Proficiency in the use of Microsoft Office Suite of tools (Outlook, Word, Excel, etc.)To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below:a) For Position in Mumbai Search : SAS + CDB Programmer Mumbai (Job Code # 83)b) For Position in Pune Search : SAS + CDB Programmer Pune (Job Code # 84)

HiWe are Hiring for ITES Company for the Pharmacovigilance Aggregate Reporting RoleJob Description: Minimum 2 - 3 years of medical writing work experience including 1 to 2 years of experience in periodic aggregate safety report writing (i.e. PBRER, PSUR, DSUR etc.) To perform all pre-DLP activities and planning for all assigned reports as per client instructions and timelines including the conducting of strategy meeting, kick-off meetings and other ad hoc report related meetings. Performs activities related to the preparation, writing and review of safety portions of Periodic Aggregate Safety Reports (PBRER, DSUR etc.) To perform compilation of all global and country specific periodic aggregate safety reports assigned by the supervisor. To perform peer review of the assigned periodic safety report and complete the corresponding QC checklists within the assigned timeline. To track and drive the progress of safety periodic reports as per the client defined timelines. To ensure compliance to SOPs (client e-manuals and training modules) and other process related documentation. Drafting and maintaining PV agreements and SDEA'S Workflow management along with case allocationAccountable for updating relevant databases, repositories, trackers and logs on an ongoing basis as per relevant SOPsSubmission of cases to various regulatory Authorities (EMA, MHRA, FDA, Health Canada)Execute drug safety data management process- a combination of case intake, triage, case entry, medical coding, narrative writing, peer review, case follow-up, report preparation- with accountability for quality and timelines of deliverables and responsibility for process improvementsMaintaining and drafting project level SOPs as per Statement of Work.Create/collate periodic reports for client report meetings. To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below:a) For Position in Mumbai Search : PV Aggregate Mumbai (Job Code # 54)b) For Position in Pune Search : PV Aggregate Pune (Job Code # 55)

We are Hiring For Leading ITES Company for the position of PV Aggregate Reporting RoleJob Descriptions To perform all pre-DLP activities and planning for all assigned reports as per client instructions and timelines including the conducting of strategy meeting, kick-off meetings and other ad hoc report related meetings. Performs activities related to the preparation, writing and review of safety portions of Periodic To perform compilation of all global and country specific periodic aggregate safety reports assigned by the supervisor. To perform peer review of the assigned periodic safety report and complete the corresponding QC checklists within the assigned timeline. To track and drive the progress of safety periodic reports as per the client defined timelines. To ensure compliance to SOPs (client e-manuals and training modules) and other process related documentation Aggregate Safety Reports (PBRER, DSUR etc.) Eligibility: Minimum 2 - 3 years of medical writing work experience including 1 to 2 years of experience in periodic aggregate safety report writing (i.e. PBRER, PSUR, DSUR etc.) Working knowledge of MS Office applications Flexibility to work as per business requirements. Understands and interprets data/information and its practical application. Knowledge of industry and business principles related to biopharmaceutical products and combination products. Good interpersonal, verbal, and written communication skillsTo Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below:a) For Position in Mumbai Search : PV Aggregate Mumbai (Job Code # 54)b) For Position in Pune Search : PV Aggregate Pune (Job Code # 55)

HiWe are Hiring for the job role of Medical Writer Job Description:* Prepare and review clinical documents that are part of regulatory submission including but not limited to Protocol, Clinical Study Pharmacology Report, Clinical Study Report, Narratives, and Post Approval Documents across the Therapeutic Areas.* Quality check of the clinical documents that are part of regulatory submission including but not limited to Protocol, Clinical Study Pharmacology Report, Clinical Study Report, Narratives, Clinical Summary of Safety, Clinical Summary of Efficacy and Common Technical Document Modules.* Initiate start up meetings with the Study Teams related to the creation and development of the clinical document for regulatory submission, if required.* To work in coordination with all the members in the study team- internal and external for the development of clinical documents.* Share project timelines amongst the study team for the development of document.* Prepare Clinical Documents according to the Standard Operating Procedures, Document Standards and Guidance document.* Review statistical analysis plans and table/figure/listing, when required.* Ensure uniformity and consistency in the scientific content of the regulatory documents* Preparation of documents in the scope and other Medical Writing documents that may be required for domestic and international regulatory submissions to the US, European, and other regulatory agencies.* Prepare Medical Writing documents within established timelines that are of high quality for scientific content, organization, clarity, accuracy, format, and consistency, with adherence to regulatory guidelines and applicable standards, styles, guidelines, and processes.* Perform peer review and quality control review of the documents within established timelines with adherence to applicable guidelines, and processes, using appropriate checklists.* Take an active role on assigned projects with respect to planning of content, format, and timing of documents, report scheduling/tracking, etc.* Provide support to the assigned clinical development or project team to ensure that project needs, and department standards are met, while completing reports within established schedules/timelines.* Plan and organize project and non-project meetings, as and when required To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below:a) For Position in Mumbai Search : Medical Writer Mumbai ( Job Code # 56)b) For Position in Pune Search : Medical Writer Pune ( Job Code # 57)

Hi, We are hiring for ITES Company for Validation Associate Role. Job description***Minimum 3 years as Validation Associate is required.***1. Data validation test script creation:Create necessary validation scenarios needed to ensure checks are functioning as required and document scenarios in the Data Validation Specification(DVS). Document expected results for each testing scenario.Feedback to the clinical Data Scientist (CDS) any ambiguities in logic that require clarification for testing scenario creation.2. Data validation test script execution: Entry of test data as specified in each testing scenario Compare the result obtained through entry of the test data to the expected result. Re-execute all checks that do not pass to ensure they are actual failure. Document validation failures. For validation failures due to incorrect testing scenarios, update DVS and re-execute testing scenario. Re-execute and document within the DVS validation results for checks that required programming updates.3. Validation of the SI data set creation process:Enter data into all study visits and forms. Extract data from InForm into SI datasetsGenerate list of data within InFormGenerate list of data contained within SI datasetsCompare InForm listing to the SI dataset listing. Document unexpected inconsistencies between listing.Review time slicing specification against the SI data sets to ensure time slicing variables are being accurately populated. Document incorrect/unexpected time slicing variable assignments.Compare the pre-defined variable values as specified in the DVS against the SI data sets. Document inconsistenciesTo Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below:a) For Position in Mumbai Search : Validation Associate Mumbai (Job Code # 171)b) For Position in Pune Search : Validation Associate Pune (Job Code # 172)C) For Position in Indore Search : Validation Associate Indore (Job Code # 174)

Hi,We are hiring for Leading ITES Company for Medical Writer Profile. Role & Responsibilities: Prepare and review clinical documents that are part of regulatory submission including but not limited to Protocol, Clinical Study Pharmacology Report, Clinical Study Report, Narratives, and Post Approval Documents across the Therapeutic Areas.Quality check of the clinical documents that are part of regulatory submission including but not limited to Protocol, Clinical Study Pharmacology Report, Clinical Study Report, Narratives, Clinical Summary of Safety, Clinical Summary of Efficacy and Common Technical Document Modules. Initiate start up meetings with the Study Teams related to the creation and development of the clinical document for regulatory submission, if required.To work in coordination with all the members in the study team- internal and external for thedevelopment of clinical documents. Share project timelines amongst the study team for the development of document.Prepare Clinical Documents according to the Standard Operating Procedures, Document Standards and Guidance document. Review statistical analysis plans and table/figure/listing, when required. Ensure uniformity and consistency in the scientific content of the regulatory documentsPreparation of documents in the scope and other Medical Writing documents that may be required for domestic and international regulatory submissions to the US, European, and other regulatory agencies. Prepare Medical Writing documents within established timelines that are of high quality for scientific content, organization, clarity, accuracy, format, and consistency, with adherence to regulatory guidelines and applicable standards, styles, guidelines, and processes. Perform peer review and quality control review of the documents within established timelines with adherence to applicable guidelines, and processes, using appropriate checklists. Take an active role on assigned projects with respect to planning of content, format, and timing of documents, report scheduling/tracking, etc. Provide support to the assigned clinical development or project team to ensure that project needs, and department standards are met, while completing reports within established schedules/timelines.Plan and organize project and non-project meetings, as and when required To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below:a) For Position in Mumbai Search : Medical Writing (Job Code # 56)b) For Position in Pune Search : Medical Writing (Job Code # 57)

HiWe are hiring for the ITES Company for the SAS : J Review Programmer RoleRole & responsibilities Programming, specifically Programming, specifically J Review, SQL, R and GitHub. Good to have SAS.Create data cleaning reporting solutions study status metric, and monitoring reports and visualizations required per standard and study specific data review plans. 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 Technical skills and experience using relational databases (e.g. MS SQL Server, Redshift, or Oracle), EDC build and/or clinical data management experience preferred Experience in AWS preferred Experience setting up automated validation is preferredKnowledge of Data lake and creating interactive Dashboards are preferredProficiency in the use of Microsoft Office Suite of tools (Outlook, Word, Excel, etc.)To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below: a) For Position in Pune Search : J Review Pune (Job Code # 89)b) For Position in Mumbai Search : J Review Mumbai (Job Code # 90)

Hi , WE are hiring for Leading ITES Company for SAS Programmer & CDB Programmer ( J Reviewer/Python/SAS)Role & responsibilities:1.Create data cleaning reporting solutions study status metric, and monitoring reports and visualizations required per standard and study specific data review plans. 2. Develop library of reusable checks working closely with data engineers and config specialists.3. Collaborate with cross functional teams in creating business rules and automated checklibrary across TAU.4. Serves as a technical resource for creating data analytics to help with data validation and cleaning.5. Provide programming expertise for data cleaning to efficiently ensure high quality data. 6. Ensure accurate delivery by creating macros for Standard listings for the department based on specifications. 7. Develop programs that generate CRF and Query metrics, including ad-hoc Sponsor andinternal programming requests. 8. Ability to set up and configure analytics for coding reports, safety review and any risk-based monitoring activities.9. 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.) 10. Understanding of regulatory requirements and relevant data standards; CDISC knowledge and experience are preferable 11. Technical skills and experience using relational databases (e.g. MS SQL Server, Redshift, or Oracle),12. EDC build and/or clinical data management experience preferred 13. Experience in AWS preferred14. Experience setting up automated validation is preferred15. Knowledge of Data lake and creating interactive Dashboards are preferred16. Proficiency in the use of Microsoft Office Suite of tools (Outlook, Word, Excel, etc.)To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below:a) For Position in Nagpur Search : SAS + CDB Programmer Nagpur (Job Code # 85)b) For Position in Bangalore Search : SAS + CDB Programmer Bangalore (Job Code # 86)

Hi We are Hiring for Leading ITES Company for the role of Statistical ProgrammerJob Description:We are looking for an associate with at least 5 - 10 years of experience for Statistical programming position, having strong understanding of SAS Base/Macros/GTL and experience of SDTM/ADAM/TLFs creation as per CDISC standards. Associate should be able to manage communication with customers, track and ensure quality on-time deliverables, suggest and drive implementation of process improvements for enhanced quality and efficiency gains, institute robust processes to ensure consistent outcomes with quicker turn-around time. Expertise in Base and Advance SAS programming. Expertise in developing macros and developing generalized programs. Development of the complex SAS macros that can be utilized across TAs in multiple studies, review of the developed SAS programs. Expertise in SQL, architecting Data Preparation, Data Visualization, Data Integration, Analytical Reporting. Worked on different SAS tools like SAS Data Integration, SAS Studio, SAS EG, SAS Management Console. SAS Developer with over 5+ years of experience with expertise on different domains. Possess solid ability in integrating programming skills, adapting to new applications and expertise in architecting Data Preparation, Data Visualization, Data Integration, Analytical Reporting. Worked on different SAS tools like SAS Data Integration, SAS Studio, SAS EG, SAS Management Console. Experience in ETL Preparation, data exploration, data preparation, data cleansing, reporting, and technical document preparation. Import /Export data using various techniques like PROC IMPORT, PROC EXPORT, LIBNAME, INFILE, PROC PRINT statements. Good Knowledge of Data management, Data handling, and Creating Data structure Knowledge of Database languages such as MYSQL, Oracle. Knowledge of various SAS Procedures like PROC Means, PROC Freq, PROC Contents, PROC Import, PROC Format, Proc Summary, PROC Sort, PROC Transpose, and PROC Report. Knowledge Of SAS procedures like SAS/Base, SAS/Macro, SAS/SQL, SAS Arrays, Do loops, SQL Joins, Hash join techniques Generating ABT and RBT tables for predictive modeling. Co-ordinate with team members to create repositories, data connections, and data jobs. Having Basic Knowledge of SAS Anti-Money Laundering like Data Model, Understanding Different Scenarios, Mapping. Good Knowledge of understanding client requirements, gathering requirements, reducing requirement error, and contributing to the team to deliver quality solutions on time and within budget. To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below:a) For Position in Nagpur Search : Statistical Programmer Nagpur (Job Code # 210)b) For Position in Bangalore Search : Statistical Programmer Bangalore (Job Code # 211)

HiWe are hiring for the ITES Company for the SAS : J Review Programmer RoleRole & responsibilities Programming, specifically Programming, specifically J Review, SQL, R and GitHub. Good to have SAS.Create data cleaning reporting solutions study status metric, and monitoring reports and visualizations required per standard and study specific data review plans. 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 Technical skills and experience using relational databases (e.g. MS SQL Server, Redshift, or Oracle), EDC build and/or clinical data management experience preferred Experience in AWS preferred Experience setting up automated validation is preferredKnowledge of Data lake and creating interactive Dashboards are preferredProficiency in the use of Microsoft Office Suite of tools (Outlook, Word, Excel, etc.)To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below:a) For Position in Bangalore Search : J Review Bangalore (Job Code # 87)b) For Position in Nagpur Search : J Review Nagpur (Job Code # 88)

Hi,We are hiring for ITES Company for Spotfire Programmer Role. Job description:Minimum 3 years of experience as a Spotfire Programmer and Clinical experience is MandatoryWorking on Refreshes requests for SRT & CSTVBuilding Oncology & Standard Visuals for Clinical Study Team Visualization (CSTV)Setting up standard and Study Specific Spotfire requests for Safety Review Team (SRT)Knowledge of Spotfire, Study configuration tool and On Demand Tool.Creating SAS Codes as per the requirementSetup and customization of visuals for Medical ReviewersValidation of visuals as per the specificationsOptimize data models and queries for improved performance and scalability.Monitor and troubleshoot issues related to the Spotfire platform and coordinate with vendors for advanced support.Seeking opportunities to leverage expertise in Spotfire development and data visualization to contribute to the success of a data-driven organization.Integrate and prepare data, create visualizations and reports, optimize performance, and collaborate with stakeholders. Possesses a strong understanding of data exploration, ETL processes, and programming in R. Adept at collaborating with clients and stakeholders to translate complex data into clear and actionable insights. To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below:a) For Position in Bangalore Search : Spotfire Programmer Bangalore (Job Code # 80)b) For Position in Ahmedabad Search : Spotfire Programmer Ahmedabad (Job Code # 82)

Hi, We are hiring for ITES Company for SDTM Programmer Role. Job description: Minimum 2 years of experience for Senior Statistical programming is a mandate.• Having strong understanding of SAS Base/Macros/GTL and experience of SDTM/ADAM/TLFs creation as per CDISC standards.• Associate should be able to manage communication with customers, track and ensure quality on-time deliverables• Implementation of process improvements for enhanced quality and efficiency gains, institute robust processes to ensure consistent outcomes with quicker turn-around time.• Experience in SDTM, ADAM & TLF• Experience in EDC & VEEVA• Expertise in Base and Advance SAS programming.• Expertise in developing macros and developing generalized programs.• Development of the complex SAS macros that can be utilized across TAs in multiple studies, review of the developed SAS programs.• Expertise in SQL, SAS Macros, Functions, SAS GTL, SAS, and other advanced SAS components.• Mentor and supervise developers to build generic standard macros, generic listings or other ad-hoc requests in accordance with business requirements Key Skills:a) Minimum 2 years of Experience in SDTM, ADAM & TLF is mustb) Any Graduate To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below: a) For Position in Bangalore Search : Job Code # 91 b) For Position in Nagpur Search : Job Code # 92

HiWe are Hiring for the ITES Company for the position of SAS: Statistical ProgrammerJob Description: We are looking for an associate with at least 5 - 10 years of experience for Statistical programming position, having strong understanding of SAS Base/Macros/GTL and experience of SDTM/ADAM/TLFs creation as per CDISC standards. Associate should be able to manage communication with customers, track and ensure quality on-time deliverables, suggest and drive implementation of process improvements for enhanced quality and efficiency gains, institute robust processes to ensure consistent outcomes with quicker turn-around time.Expertise in Base and Advance SAS programming. Expertise in developing macros and developing generalized programs. Development of the complex SAS macros that can be utilized across TAs in multiple studies, review of the developed SAS programs.Expertise in SQL, architecting Data Preparation, Data Visualization, Data Integration, Analytical Reporting. Worked on different SAS tools like SAS Data Integration, SAS Studio, SAS EG, SAS Management Console. SAS Developer with over 5+ years of experience with expertise on different domains. Possess solid ability in integrating programming skills, adapting to new applications and expertise in architecting Data Preparation, Data Visualization, Data Integration, Analytical Reporting. Worked on different SAS tools like SAS Data Integration, SAS Studio, SAS EG, SAS Management Console. Experience in ETL Preparation, data exploration, data preparation, data cleansing, reporting, and technical document preparation. Import /Export data using various techniques like PROC IMPORT, PROC EXPORT, LIBNAME, INFILE, PROC PRINT statements. Good Knowledge of Data management, Data handling, and Creating Data structure Knowledge of Database languages such as MYSQL, Oracle. Knowledge of various SAS Procedures like PROC Means, PROC Freq, PROC Contents, PROC Import, PROC Format, Proc Summary, PROC Sort, PROC Transpose, and PROC Report. Knowledge Of SAS procedures like SAS/Base, SAS/Macro, SAS/SQL, SAS Arrays, Do loops, SQL Joins, Hash join techniques To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below:a) For Position in Nagpur Search : Statistical Programmer Nagpur (Job Code # 210)b) For Position in Bangalore Search : Statistical Programmer Bangalore (Job Code # 211)

HiWe are hiring for Leading ITES Company for SAS+R Programmer Profile.Role & responsibilities: a) Any Graduateb) Minimum of 3 years of experience in SAS + R programming c) Familiarity with data visualization techniques and tools in Rd) CDISC knowledge & experienceRoles & 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 knowledgeDevelop 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 # 375b) For Position in Hyderabad Search : Job Code # 376

Hi, We are hiring for ITES Company for Validation Associate Role. Job description***Minimum 3 years as Validation Associate is required.***1. Data validation test script creation:Create necessary validation scenarios needed to ensure checks are functioning as required and document scenarios in the Data Validation Specification(DVS). Document expected results for each testing scenario.Feedback to the clinical Data Scientist (CDS) any ambiguities in logic that require clarification for testing scenario creation.2. Data validation test script execution: Entry of test data as specified in each testing scenario Compare the result obtained through entry of the test data to the expected result. Re-execute all checks that do not pass to ensure they are actual failure. Document validation failures. For validation failures due to incorrect testing scenarios, update DVS and re-execute testing scenario. Re-execute and document within the DVS validation results for checks that required programming updates.3. Validation of the SI data set creation process:Enter data into all study visits and forms. Extract data from InForm into SI datasetsGenerate list of data within InFormGenerate list of data contained within SI datasetsCompare InForm listing to the SI dataset listing. Document unexpected inconsistencies between listing.Review time slicing specification against the SI data sets to ensure time slicing variables are being accurately populated. Document incorrect/unexpected time slicing variable assignments.Compare the pre-defined variable values as specified in the DVS against the SI data sets. Document inconsistenciesTo Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below:a) For Position in Bangalore Search : Validation Associate Bangalore (Job Code # 173)b) For Position in Ahmedabad Search : Validation Associate Ahmedabad (Job Code # 175)

Hi, We are hiring for the Leading ITES Company for Human Resources- US / Canada / UK Payroll Profile.Job description: Overall work experience of 6+ years in Payroll domain specifically managing all areas within Payroll Transaction services scope as well as Payroll integration with Time and HCM systemsExperience in handling Clients:Escalations and reviews as well as daily interactions.Should have interacted with Customer for metrics and trackingShould have handled a team of 8+ associates for a clientAbility to communicate with upstream and downstream payroll partners and other vendors to drive day to day operations.Preferred experience of handling client escalationsPreferred experience on Payroll regulations for countriesPreferable experience on multiple Payroll systemsPreferred experience on managing Payroll QueriesSkills1) Excellent Communication Skills2) MS Office & Excel Skills3) Customer Management Skills4) Presentation Skills5) Coaching Skills Preferred Skills a) Should have handled a team of 8+ associates for a clientb) Experience in US/Canada Payrollc) Experience on managing Payroll Queriesd) Experience on Payroll regulations for countriese) Any Graduate To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below: a) For Position in Bangalore Search for US Payroll : Job Code # 387 b) For Position in Bangalore Search for Canada Payroll : Job Code # 388 c) For Position in Bangalore Search for UK Payroll : Job Code # 389

Hi, We are hiring for ITES Company for SAS + CDB Programmer Role. Job description:Programming, specifically J Review, SQL, R and GitHub. Good to have Python. Create data cleaning reporting solutions study status metric, and monitoring reports and visualizations required per standard and study specific data review plans. 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 Technical skills and experience using relational databases (e.g. MS SQL Server, Redshift, or Oracle), EDC build and/or clinical data management experience preferred Experience in AWS preferred Experience setting up automated validation is preferred Knowledge of Data base and creating interactive Dashboards are preferred Proficiency in the use of Microsoft Office Suite of tools (Outlook, Word, Excel, etc.) Key Skills:a) Minimum 3 years of Experience in SAS CDB Programmers with R programming.b) Good to have Python knowledgec) Any Graduate To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below: a) For Position in Mumbai Search : Job Code # 83

HiWe are looking to hire for SAS+R Programming. Please go through the JD and ApplyRoles & 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 Rpackages (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 Rprogramming validation. Strong proficiency in R programming, including data manipulation, statisticalanalysis, 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 configspecialists. Collaborate with cross functional teams in creating business rules and automatedcheck library across TAU. Serves as a technical resource for creating data analytics to help with datavalidation and cleaning. Provide programming expertise for data cleaning to efficiently ensure high qualitydata. Ensure accurate delivery by creating macros for Standard listings for thedepartment based on specifications. Develop programs that generate CRF and Query metrics, including ad-hoc Sponsorand internal programming requests. Ability to set up and configure analytics for coding reports, safety review and anyrisk-based monitoring activities. Operational experience in pharmaceutical drug development with significant directexposure to clinical development and data operations required for the reporting ofclinical trial data (e.g. data review, regulatory submissions, safety updates, etc.) Understanding of regulatory requirements and relevant data standards; CDISCknowledge and experience are preferable.To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below:a) For Position in Bangalore Search : Job Code # 375b) For Position in Hyderabad Search : Job Code # 376

HiWe are Hiring Leading ITES Company for Medical Reviewer Role. Please go through the JD and Apply Job Description: Author a company clinical comment (CCC) for case reports that are Suspected Unexpected Serious Adverse reaction (SUSAR). Edit the Periodic Report Comment, if applicable, directly within the Periodic Report Comment field in the Patient Safety database. Perform the following actions within the Comments field of the GSP Review Workflow step in the Patient Safety database: -Review and respond to any queries/comments from the Case Owner, which are recorded in the Comment field of the GSP Review Workflow step in the Patient Safety database. -Detail any requests for changes to the case, including the narrative. -Detail any follow-up information that is required and not already noted within the Query Manager in the Patient Safety database. Provide product advice as required, especially with regards to case reports that are Suspected Unexpected Serious Adverse reaction (SUSAR). Review the company causality assessment provided by Medical Advisor. Review the medical sense including seriousness and coding of the case in the global context of the drug or clinical project, including the narrative, AE/SAE terms, suspect drugs, concomitant medications, laboratory data, and medical history. To provide documentation of the review and case comments in Sapphire in Medical Review workflow. Ensure compliance with global and local procedural documents and local implementation of client Maintain knowledge of the marketed drug currently under litigation. Maintain knowledge of the company disease and therapeutic areas for marketed drugs and drugs in development through periodic medical review training held by client medical staff. To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below:a) For Position in Nagpur Search : Job Code # 49b) For Position in Gandhinagar Search : Job Code # 50c) For Position in Bangalore Search : Job Code # 51

Hi,We are hiring for Leading ITES Company for Lead Data Manager Profile. Job DescriptionPerform day to day Clinical Data Management activities.Work and coordinate with the team to perform data management activities and deliver an error free quality database in accordance with the data management plan and regulator standards.Read and understand the study protocol and the timelines.Perform test data entry in TEST environment, data listing review, data reconciliation and query management tasks. Escalate/Action discrepancy in the clinical data as appropriate.Perform external checks to handle manual discrepancies and action the same.Ensure an error free, quality data with no open queries.Escalate any discrepancy in the clinical data to the study lead as appropriate.Timely completion of trainingsAny other tasks deemed appropriateTo perform medical data collection and analysis of Prostate Cancer Data using databases like HIS/ EMR (Electronic Medical Record) and Cases Rave, CDM (startup, close out, conduct)Client interaction and meetings.Bringing up new ideas and executing new plans to cope with the back-log.Training to new team members as and when required. Key Skills:a) Minimum 3 years of Experience in leading clinical studies/ Clinical Data Managementb) Hands on experience of Study Conduct and Close Out is mustc) Any Graduate To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below:a) For Position in Pune Search : Job Code # 96b) For Position in Nagpur Search : Job Code # 97

Hi, We are hiring for the ITES Company for Fare Filing Distribution Role.Job description: Minimum 1-year experience in a Fare Filing Distribution Role is mandatory.Possess knowledge of filing and updating fares in the ATPCO system based on the information provided.Possess knowledge of filing and updating rule conditions such as Eligibility, Date/Time, Seasonality, Flight Application, Combinations, Advance Purchase, Negotiated Fares, Surcharge, Blackout, Automated Changes and Cancellation, Fare By Rule, Footnote, Routing Map, etc. in the ATPCO system based on the information provided.Possess knowledge of special fare filing activities such as YQ/YR, Optional and Ancillary services, Branded Fares, Chart 1 & 2.Possess knowledge of performing quality assurance checks in the Global Distribution Systems (GDS) such as Amadeus, Galileo, Sabre, etc.Should be well conversant with all the fare pricing and troubleshooting entries in the GDS such as Amadeus, Galileo, Sabre, etc.Good knowledge of World Geography, Fare Construction, etc.Validate fares and rules data for accuracy, completeness, and consistency.Identify fare and rule inconsistencies in the ATPCO and GDS systems.Stay updated with industry trends and changes in ATPCO procedures Preferred Skills:a) Minimum 1-year experience in a Fare Filing Distributionb) Experience of fare pricing and troubleshooting entries in the GDS such as Amadeus, Galileo, Sabre, etcc) Any Graduate To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below:a) For Position in Pune Search : Job Code # 393

US MNC IN GURGAON IS HIRING FOR A CUSTOMER SUPPORT PROCESSDaily Walkin @ Outpace Consulting, C-29, Sec 2 Noida (Nearest Metro Noida Sec 15, Exit Gate 3)Landmark : Near Hotel NirulasKhushboo @ 9793988034, Sanchita @ 9532132502, Inderpreet @ 9026440584Whatsapp Your CV to 9721919721 Job Details:1: Graduate/UG Freshers2: Candidate Must Not Have Any Exams in Next 6 Months3: 24x7 Shifts4: Customer Support: Non-Voice/Blended/Voice5: 5 Days Working6: Sal 2.5 to 3.6 LPA + Travel Allowance (2500) + Incentives7: Excellent Communication Skills8: Cabs Available in odd hours9: Immediate Joiners

US MNC IN GURGAON IS HIRING FOR A CUSTOMER SUPPORT PROCESSDaily Walkin @ Outpace Consulting, C-29, Sec 2 Noida (Nearest Metro Noida Sec 15, Exit Gate 3)Landmark : Near Hotel NirulasKhushboo @ 9793988034, Sanchita @ 9532132502, Inderpreet @ 9026440584Whatsapp Your CV to 9721919721 Job Details:1: Graduate/UG Freshers2: Candidate Must Not Have Any Exams in Next 6 Months3: 24x7 Shifts4: Customer Support: Non-Voice/Blended/Voice5: 5 Days Working6: Sal 2.5 to 3.6 LPA + Travel Allowance (2500) + Incentives7: Excellent Communication Skills8: Cabs Available in odd hours9: Immediate Joiners

US MNC IN GURGAON IS HIRING FOR A CUSTOMER SUPPORT PROCESSDaily Walkin @ Outpace Consulting, C-29, Sec 2 Noida (Nearest Metro Noida Sec 15, Exit Gate 3)Landmark : Near Hotel NirulasKhushboo @ 9793988034, Sanchita @ 9532132502, Inderpreet @ 9026440584Whatsapp Your CV to 9721919721 Job Details:1: Graduate/UG Freshers2: Candidate Must Not Have Any Exams in Next 6 Months3: 24x7 Shifts4: Customer Support: Non-Voice/Blended/Voice5: 5 Days Working6: Sal 2.5 to 3.6 LPA + Travel Allowance (2500) + Incentives7: Excellent Communication Skills8: Cabs Available in odd hours9: Immediate Joiners

US MNC IN GURGAON IS HIRING FOR A CUSTOMER SUPPORT PROCESSDaily Walkin @ Outpace Consulting, C-29, Sec 2 Noida (Nearest Metro Noida Sec 15, Exit Gate 3)Landmark : Near Hotel NirulasKhushboo @ 9793988034, Sanchita @ 9532132502, Inderpreet @ 9026440584Whatsapp Your CV to 9721919721 Job Details:1: Graduate/UG Freshers2: Candidate Must Not Have Any Exams in Next 6 Months3: 24x7 Shifts4: Customer Support: Non-Voice/Blended/Voice5: 5 Days Working6: Sal 2.5 to 3.6 LPA + Travel Allowance (2500) + Incentives7: Excellent Communication Skills8: Cabs Available in odd hours9: Immediate Joiners

US MNC IN GURGAON IS HIRING FOR A CUSTOMER SUPPORT PROCESSDaily Walkin @ Outpace Consulting, C-29, Sec 2 Noida (Nearest Metro Noida Sec 15, Exit Gate 3)Landmark : Near Hotel NirulasKhushboo @ 9793988034, Sanchita @ 9532132502, Inderpreet @ 9026440584Whatsapp Your CV to 9721919721 Job Details:1: Graduate/UG Freshers2: Candidate Must Not Have Any Exams in Next 6 Months3: 24x7 Shifts4: Customer Support: Non-Voice/Blended/Voice5: 5 Days Working6: Sal 2.5 to 3.6 LPA + Travel Allowance (2500) + Incentives7: Excellent Communication Skills8: Cabs Available in odd hours9: Immediate Joiners

US MNC IN GURGAON IS HIRING FOR A CUSTOMER SUPPORT PROCESSDaily Walkin @ Outpace Consulting, C-29, Sec 2 Noida (Nearest Metro Noida Sec 15, Exit Gate 3)Landmark : Near Hotel NirulasKhushboo @ 9793988034, Sanchita @ 9532132502, Inderpreet @ 9026440584Whatsapp Your CV to 9721919721 Job Details:1: Graduate/UG Freshers2: Candidate Must Not Have Any Exams in Next 6 Months3: 24x7 Shifts4: Customer Support: Non-Voice/Blended/Voice5: 5 Days Working6: Sal 2.5 to 3.6 LPA + Travel Allowance (2500) + Incentives7: Excellent Communication Skills8: Cabs Available in odd hours9: Immediate Joiners

US MNC IN GURGAON IS HIRING FOR A CUSTOMER SUPPORT PROCESSDaily Walkin @ Outpace Consulting, C-29, Sec 2 Noida (Nearest Metro Noida Sec 15, Exit Gate 3)Landmark : Near Hotel NirulasKhushboo @ 9793988034, Sanchita @ 9532132502, Inderpreet @ 9026440584Whatsapp Your CV to 9721919721 Job Details:1: Graduate/UG Freshers2: Candidate Must Not Have Any Exams in Next 6 Months3: 24x7 Shifts4: Customer Support: Non-Voice/Blended/Voice5: 5 Days Working6: Sal 2.5 to 3.6 LPA + Travel Allowance (2500) + Incentives7: Excellent Communication Skills8: Cabs Available in odd hours9: Immediate Joiners

US MNC IN GURGAON IS HIRING FOR A CUSTOMER SUPPORT PROCESSDaily Walkin @ Outpace Consulting, C-29, Sec 2 Noida (Nearest Metro Noida Sec 15, Exit Gate 3)Landmark : Near Hotel NirulasKhushboo @ 9793988034, Sanchita @ 9532132502, Inderpreet @ 9026440584Whatsapp Your CV to 9721919721 Job Details:1: Graduate/UG Freshers2: Candidate Must Not Have Any Exams in Next 6 Months3: 24x7 Shifts4: Customer Support: Non-Voice/Blended/Voice5: 5 Days Working6: Sal 2.5 to 3.6 LPA + Travel Allowance (2500) + Incentives7: Excellent Communication Skills8: Cabs Available in odd hours9: Immediate Joiners

US MNC IN GURGAON IS HIRING FOR A CUSTOMER SUPPORT PROCESSDaily Walkin @ Outpace Consulting, C-29, Sec 2 Noida (Nearest Metro Noida Sec 15, Exit Gate 3)Landmark : Near Hotel NirulasKhushboo @ 9793988034, Sanchita @ 9532132502, Inderpreet @ 9026440584Whatsapp Your CV to 9721919721 Job Details:1: Graduate/UG Freshers2: Candidate Must Not Have Any Exams in Next 6 Months3: 24x7 Shifts4: Customer Support: Non-Voice/Blended/Voice5: 5 Days Working6: Sal 2.5 to 3.6 LPA + Travel Allowance (2500) + Incentives7: Excellent Communication Skills8: Cabs Available in odd hours9: Immediate Joiners

US MNC IN GURGAON IS HIRING FOR A CUSTOMER SUPPORT PROCESSDaily Walkin @ Outpace Consulting, C-29, Sec 2 Noida (Nearest Metro Noida Sec 15, Exit Gate 3)Landmark : Near Hotel NirulasKhushboo @ 9793988034, Sanchita @ 9532132502, Inderpreet @ 9026440584Whatsapp Your CV to 9721919721 Job Details:1: Graduate/UG Freshers2: Candidate Must Not Have Any Exams in Next 6 Months3: 24x7 Shifts4: Customer Support: Non-Voice/Blended/Voice5: 5 Days Working6: Sal 2.5 to 3.6 LPA + Travel Allowance (2500) + Incentives7: Excellent Communication Skills8: Cabs Available in odd hours9: Immediate Joiners

Hi, We are hiring for Leading ITES Company for R Biostatistical Programmer Lead Profile.Job Description:Minimum 9 + years of experience with Pharmaceutical or CRO industry engaged in Clinical and Preclinical Research Good understanding of applied statistical principles and modeling in the design and analysis of clinical studies Good understanding of ICH and regulatory guidelines Experience in CDISC SDTM and Adam standards Good knowledge and hands on experience in Base SAS, SAS / STAT, SAS /Graph modules and R Statistical programming.Good communication and interpersonal skillsExperience in handling domain interactions with the customer.Preferred Educational Qualification for the role: Masters or Doctorate level degree in Biostatistics, Statistics, Mathematics or related fields .Essential Experience for the Role :Good knowledge and hands on experience in R and SAS Statistical Programming in Clinical DomainTo Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below:a) For Position in Hyderabad Search : Job Code # 294b) For Position in Chennai Search : Job Code # 295c) For Position in Indore Search : Job Code # 296

Hiring for Leading ITES Company In Gurgaon/Noida for Customer Support Requirements:Min 1 Year BPO/Customer Service ExperienceDaily Walkin @ Outpace Consulting, C-29, Sec 2 Noida (Nearest Metro Noida Sec 15, Exit Gate 3)Landmark : Near Hotel NirulasWalkin Time : 11 am to 4 PmCall : Arya @ 7307122569Whatsapp Your CV @ 9721919721Job Details:1: Graduate/UG With Min 1 Year Exp in Customer Support2: Candidate Must Not Have Any Exams in the Next 6 Months3: Rotational Shifts4: Customer Support 5: 5 Days Working6: Max 5.5 LPA7: Excellent Communication Skills8: Immediate Joiners Preferred

Hiring for Leading ITES Company In Gurgaon/Noida for Customer Support Requirements:Min 1 Year BPO/Customer Service ExperienceDaily Walkin @ Outpace Consulting, C-29, Sec 2 Noida (Nearest Metro Noida Sec 15, Exit Gate 3)Landmark : Near Hotel NirulasWalkin Time : 11 am to 4 PmCall : Arya @ 7307122569Whatsapp Your CV @ 9721919721Job Details:1: Graduate/UG With Min 1 Year Exp in Customer Support2: Candidate Must Not Have Any Exams in the Next 6 Months3: Rotational Shifts4: Customer Support 5: 5 Days Working6: Max 5.5 LPA7: Excellent Communication Skills8: Immediate Joiners Preferred

Hi,We are Hiring For ITES Company For Order Management Role.Job Description:Overall 8+ years of Experience in Order Management with minimum 2 years in PO Creation in Retails IndustryDaily Report Retrieval (Hot Report, Short Report and others) via QMF (query managementframework) SQL editorLoading SKU External Forecasts and Conducting Plan Analysis in JDAGenerating Supplementary Orders for FIRM Orders and OTBReviewing Bouncers and Addressing DiscrepanciesMake recommendations for investment buy options.Monitoring performance using Key Performance Indicators (KPIs).Regular discussions and collaboration with stakeholders Skill Set:1) Experience in Report consolidation and Summary Generation2) Proficiency in Excel and Macro Creation (SQL & VB Scripts)3) Good Analytical Skill4) Experience in JDA5) Good Communication and Presentation Skills Preferred Skills:a) Minimum 2 Years of Experience in Retail Industryb) Buyer Role Experiencec) PO creation Experienced) Any Graduate To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below:a) For Position in Chennai Search : Job Code # 381 b) For Position in Nagpur Search : Job Code # 382

Hiring for Leading ITES Company In Gurgaon for Chat Support Requirements:Min 1 Year International Chat Experience MandatoryDaily Walkin @ Outpace Consulting, C-29, Sec 2 Noida (Nearest Metro Noida Sec 15, Exit Gate 3)Landmark : Near Hotel NirulasCall Arya @ 7307122569Whatsapp : 9721919721Job Description & Specifications:1: Graduate/UG With Min 1 Year Exp in Customer Support - International Chat2: Candidates need to support customer queries through Chat Support3: Process Deals with a Leading US Based Telecom Company4: Excellent English Proficiency Required (Spoken and Written)5: Candidate Must Not Have Any Exams in the Next 6 Months6: Rostered Shifts7: 2 Week offs (Rostered)8: 5 Days Working9: Sal Max 35K10: Incentives 2.5K (Performance Based)11: Cabs During odd hours (7 pm to 7 am)

Hiring for Leading ITES Company In Gurgaon for Chat Support Requirements:Min 1 Year International Chat Experience MandatoryDaily Walkin @ Outpace Consulting, C-29, Sec 2 Noida (Nearest Metro Noida Sec 15, Exit Gate 3)Landmark : Near Hotel NirulasCall Arya @ 7307122569Whatsapp : 9721919721Job Description & Specifications:1: Graduate/UG With Min 1 Year Exp in Customer Support - International Chat2: Candidates need to support customer queries through Chat Support3: Process Deals with a Leading US Based Telecom Company4: Excellent English Proficiency Required (Spoken and Written)5: Candidate Must Not Have Any Exams in the Next 6 Months6: Rostered Shifts7: 2 Week offs (Rostered)8: 5 Days Working9: Sal Max 35K10: Incentives 2.5K (Performance Based)11: Cabs During odd hours (7 pm to 7 am)