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

Hiring for Leading ITES Company In 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 With Min 1 Year Exp in Customer Support2: Candidate Must Not Have Any Exams in the Next 6 Months3: Rotational Shifts (Day Shifts For Females)4: Customer Support 5: 5 Days Working6: Salary 26500 in Hand + 4000 TA + Incentives7: 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

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)

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/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 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 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 With Min 1 Year Exp in Customer Support2: Candidate Must Not Have Any Exams in the Next 6 Months3: Rotational Shifts (Day Shifts For Females)4: Customer Support 5: 5 Days Working6: Salary 26500 in Hand + 4000 TA + Incentives7: 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

Hiring for Leading ITES Company In 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 With Min 1 Year Exp in Customer Support2: Candidate Must Not Have Any Exams in the Next 6 Months3: Rotational Shifts (Day Shifts For Females)4: Customer Support 5: 5 Days Working6: Salary 26500 in Hand + 4000 TA + Incentives7: 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

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

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 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 With Min 1 Year Exp in Customer Support2: Candidate Must Not Have Any Exams in the Next 6 Months3: Rotational Shifts (Day Shifts For Females)4: Customer Support 5: 5 Days Working6: Salary 26500 in Hand + 4000 TA + Incentives7: Excellent Communication Skills8: Immediate Joiners Preferred

Hi,We are looking to hire someone for Study Data Manager Please go through the JD, we shall call back the relevant Profilesa) Experience in leading clinical studies. b) Experience on Study Conduct and Close Out JOB DECSRIPTION: Need exposure to Inform or Medidata Rave database • Responsible & Accountable for the assigned study conduct activities, in clinical trials • Validate clinical trial data to ensure consistency, integrity, and accuracy based on project-specific guidelines. • Generate data queries based on validation checks or raise Manual queries to resolve data inconsistencies. • To perform reconciliation of data from external sources (e.g. Serious Adverse Events, IWRS, Central Laboratory). • SPOC for the study communications • Proactively highlight any risks associated with the study along with the mitigation plan. • Establish a partnership with the stakeholders at the operational level to work seamlessly to deliver the assigned project/activity as per timelines. • Identify process Improvement opportunities and ensure learning is shared • Ensure deliverables and/or agreed activities/tasks with customers. are completed with the expected quality. • Have worked on Study set-up, Study Conduct, and Study Closeout for various therapeutic areas. • Have also worked on writing edit check specifications, CRF completion guidelines, and review and corrections of set-up documents for different versionsTo Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below:a) For Position in Mumbai Search : Job Code # 184b) For Position in Pune Search : Job Code # 185C) For Position in Bangalore Search : Job Code # 186

Hi We're hiring for Leading ITES Company for EDC (Veeva Programmer) RoleExperience in EDC & Veeva is Must.Job Description : Create eCRF specifications, design, develop and unit test and functionally validate clinical trial setup process Create edit check specifications and program or modify checks at study level within EDC Setup different instances of study URL (e.g.: UAT (User Acceptance Testing), production, testing etc.,)) Setup and configure user accounts for study teams Setup and manage blinded and unblinded study configurations Be the SME (Subject Matter Expert) for all database related activities Setup, configure, unit test and functionally validate and integrate other modules within the EDC ecosystem such as coding, integration of IRT, safety system, local labs etc., Familiar with custom functions within EDC systems Work closely with EDC vendors regarding any tool related issues in the system Ability to troubleshoot database setup as per study needs Prepare, test and implement postproduction changes as per study needs Archive and retire the study URL after database lock Partner with appropriate team members to establish technology standards and governance models Establish and support business process SOPs. Oversee system delivery life cycle in collaboration with appropriate partners including Clinical Operations, Clinical Supplies, IT (Information Technology), and Quality organizations Be a primary change agent to ensure adoption of new capabilities and business process Be the contact for Clinical Technology vendors to ensure established milestones are met with the highest degree of quality. Work with leaders to resolve issues affecting the delivery of clinical trials Collaborate with standards team in creating standard CRF libraries for study level consumption Work closely with data engineers and data management programmers at study level integration and delivery Lead technology vendor oversight activities. Be a process expert for operational and oversight models. Partner with appropriate team members, technology vendors, and CRO partners to avoid and resolve risks. Confirm archival and inspection readiness of all Clinical Technology Trial Master File (TMF) documents Participate in preparing function for submission readiness and may represent Clinical Information Operations (CIO) group in a formal inspection or audit. Track study deliverables and evaluate study metrics to mitigate risk for major data management deliverables. Adaptable to new ways of working using technology to accelerate clinical trial setupEducation and Experience Requirements: Bachelor's degree or related experience. Knowledge of drug development process. Minimum of 4+ years experience in Data Management, Programming, Clinical IT, or other Clinical Research related fields. Hands-on experience with at least one EDC system (e.g.: Medidata Rave, Inform, Veeva etc.,) Experience programming in CQL, working with JSON format and/or C# is preferred Experience integrating other clinical trial modules (e.g.: lab, safety, IRT, coding etc.,) with the EDC system Understanding of industry standard technologies to support Clinical Development needs (e.g., CTMS, SAS, R or Python, Data Warehouses, SharePoint) To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below:a) For Position in Mumbai Search : EDC Veeva & Inform Programmer Mumbai (Job Code # 181) b) For Position in Pune Search : EDC Veeva & Inform Programmer Pune (Job Code # 182)c) For Position in Bangalore Search : EDC Veeva & Inform Programmer Bangalore (Job Code # 183)

HiWe are hiring for Leading ITES Company for Clinical Data Manager Profile.Role & responsibilities: Candidate should have 2-5 years of experience of CDM with experience in Conduct Scope of workPerform 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 the 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 trainingAny other tasks deemed appropriateTo perform medical data collection and analysis of Prostate Cancer Data using databases like HIS/ EMR (Electronic Medical Record) and Caisis, Rave, CDM (startup, closeout, conduct) Client interaction and meetings. Bringing up new ideas and executing new plans to cope with the backlog. Training new team members as and when required.To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below:a) For Position in Mumbai Search : Job Code # 205b) For Position in Pune Search : Job Code # 206C) For Position in Bangalore Search : Job Code # 207

Hi,We are hiring for Leading ITES Company for Lead Study Data Manager ProfileSkills:a) Minimum 5 Years of Core Clinical Data Management Experience with minimum 1 year of experience of leading a clinical trial. . b) Experience on Study Conduct and Close Out c) Any GraduateJOB DECSRIPTION:Need exposure of Inform or Medidata Rave databaseResponsible & Accountable for the assigned study conduct activities, in clinical trialsValidate clinical trial data to ensure consistency, integrity and accuracy based on project specific guidelines.Generate data queries based on validation checks or raise Manual queries to resolve data inconsistencies.To perform reconciliation of data from external sources (e.g. Serious Adverse Events,IWRS, Central Laboratory).SPOC for the study communicationsProactively highlight any risks associated with the study along with the mitigation plan.Establish a partnership with the stakeholders at operational level to work seamlessly to deliver the assigned project/activity as per timelines.Identify process Improvement opportunities and to ensure learning is sharedEnsure deliverables and/or agreed activities/tasks with customer. are completed with the expected quality.Have worked on Study set-up, Study Conduct and Study Close out for various therapeutic areas. Have also worked on writing edit check specification, CRF completion guidelines and review and corrections of set up documents for different versions. To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below: a) For Position in Mumbai Search : Job Code # 184b) For Position in Pune Search : Job Code # 185c) For Position in Bangalore Search : Job Code # 186

HiWe are hiring for Leading ITES Company for Clinical Data Manager Profile.Role & responsibilities: Candidate should have 2-5 years of experience of Clinical Data Manage (CDM) with experience in Conduct Scope of workPerform 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 the 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 trainingAny other tasks deemed appropriateTo perform medical data collection and analysis of Prostate Cancer Data using databases like HIS/ EMR (Electronic Medical Record) and Caisis, Rave, CDM (startup, closeout, conduct)Client interaction and meetings. Bringing up new ideas and executing new plans to cope with the backlog. Training new team members as and when required.To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below:a) For Position in Mumbai Search : Job Code # 205b) For Position in Pune Search : Job Code # 206C) For Position in Bangalore Search : Job Code # 207

HiWe are hiring for Leading ITES Company for Clinical Data Manager Profile. Role & Responsibilities: Candidate should have 2-5 years of experience of CDM with experience in Conduct Scope of workPerform 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 the 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 trainingAny other tasks deemed appropriateTo perform medical data collection and analysis of Prostate Cancer Data using databases like HIS/ EMR (Electronic Medical Record) and Caisis, Rave, CDM (startup, closeout, conduct) Client interaction and meetings. Bringing up new ideas and executing new plans to cope with the backlog. Training new team members as and when required.To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below:a) For Position in Mumbai Search : Job Code # 205b) For Position in Pune Search : Job Code # 206C) For Position in Bangalore Search : Job Code # 207

Hi, We are hiring for Leading ITES Company for Data Management Study Point of Contact (DMSPOC) Profile.Job Description:To provide end to end data management services and project management of studies.Ensure compliance with SOPs and training.Primary point of escalation for issue management.Accountable for DM deliverables (including quality and timing) on the project and will be required to provide regular status updates on data completeness, cleanliness to the Data Manager.Point of contact for client POC.Attend meetings with Study Lead Data Manager (SLDM) as and when required, provide inputs to the required documents and activities throughout the course of the trial.Ensure that the timelines & quality are met as per study requirement.Resource estimation for the study and ensuring right resources are available for the study based on requirement.To oversight the end-to-end data management activities for assigned studies.Risk identification, mitigation and issue escalation to the appropriate stakeholders.Skillsets required:Ability to represent Data Management at all levels and is capable of targeting information to the respective audience.Ability to influence key project roles or Study Team members to meet the overall goal of the study.Ability to build influential networks with client and stakeholder management.Ability to develop solutions for cross functional challenges.Develops recommendations beyond own area of expertise.Knowledge of ICH GCP & CDISC requirements. To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below:a) For Position in Mumbai Search : Job Code # 297b) For Position in Pune Search : Job Code # 298c) For Position in Bangalore Search : Job Code # 299

Hi,We are hiring for the leading ITES Company for EDC (Veeva & Inform Programmer) Role.JOB DESCRIPTION:Create eCRF specifications, design, develop and unit test and functionally validate clinical trial setup process Create edit check specifications and program or modify checks at study level within EDC Setup different instances of study URL (e.g.: UAT (User Acceptance Testing), production, testing etc.,) Setup and configure user accounts for study teams Setup and manage blinded and unblinded study configurations Be the SME (Subject Matter Expert) for all database related activities Setup, configure, unit test and functionally validate and integrate other modules within the EDC ecosystem such as coding, integration of IRT, safety system, local labs etc., Familiar with custom functions within EDC systems Work closely with EDC vendors regarding any tool related issues in the system Ability to troubleshoot database setup as per study needs Prepare, test and implement postproduction changes as per study needs Archive and retire the study URL after database lock Partner with appropriate team members to establish technology standards and governance models • Establish and support business process SOPs. Oversee system delivery life cycle in collaboration with appropriate partners including Clinical Operations, Clinical Supplies, IT (Information Technology), and Quality organizations Be a primary change agent to ensure adoption of new capabilities and business process Be the contact for Clinical Technology vendors to ensure established milestones are met with the highest degree of quality. Work with leaders to resolve issues affecting the delivery of clinical trials Collaborate with standards team in creating standard CRF libraries for study level consumptionWork closely with data engineers and data management programmers at study level integration and delivery Lead technology vendor oversight activities. Be a process expert for operational and oversight models. To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below:a) For Position in Mumbai Search :EDC Veeva Mumbai (Job Code # 181)b) For Position in Pune Search : EDC Veeva Pune (Job Code # 182)C) For Position in Bangalore Search : EDC Veeva Bangalore (Job Code # 183)

HiWe are looking to hire Medical Data Reviewer for our Client. Please go through the JD and Apply.Responsibilities: Review subject/ patient level data for accuracy, to identify any anomalies, trends inpatient reported data Review and provide inputs ion design of eCRF Review investigation product dosing Review all reported Adverse Events (AEs), Concomitant Medication and medical Ensure that any out of range data/ anomaly is verified Review all laboratory data on study subjects Review data in the form of visualizations and identify potential issues of concernTraining new team membersQualifications: Bachelor/ Masters degree or equivalent in Life sciences/ Alternative Medicine(preferred)Eligibility: Good English communication skills Experience of handling clinical trial/ safety data - > 4 yearsTo Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below:a) For Position in Mumbai Search : Job Code # 359b) For Position in Pune Search : Job Code # 360c) For Position in Bangalore Search : Job Code # 361

HiWe are hiring for Regulatory Submissions Publisher. Job Purpose:Build and process submission dossiers of low-to-moderate complexity: Submission Dossiers that may be periodic (e.g.: safety reports) or minor amendments (e.g.: IND Amendment, DMF Amendment, CMC Update as appropriate to level, etc) or otherwise not major applications but in support of pending approvals or lifecycle commitments for marketed products(e.g.: meeting packages, responses as appropriate, Advertising and Promotion Submissions, routine labeling updates as appropriate, etc.) QC submission dossiers or parts of submission dossier output of low-to-moderate and moderate-to-high complexities as assigned. Other submission related requests could be assigned that are in support of general publishing but commensurate with role expectations.Role and Responsibilities: Utilize current electronic document management and publishing tools to prepare submission-ready Regulatory components and assemble, publish, and dispatch dossiers according to regulatory requirements for paper and electronic submissions with limited supervision Provide GRA component-level publishing support to ensure submission components conform to e-submission standards (e.g., templates, scanning, indexing) QC electronic and paper submissions to ensure compliance with company and agency requirements.Maintain effective interactions with all publishing contributors and responsible RA professionals, to ensure timely delivery of dossier components taking into consideration special requirements and needs; Maintain open and timely communication; Determine the scope of the electronic publishing requirements for the dossier Apply appropriate JRD document and dossier standards, including adherence to a pre-established submission content plan Participate in special projects and process improvement initiatives. Global Regulatory knowledge of product registration procedures covering IND, NDAs, CTAs, BLA, IMPDs, MAAs for various countries including regulated markets like US, EU, Canada and Australia-NZ. Support regulatory submissions publishing for EDMF, COS/CEP for Drug substance related filing and regulatory submissions publishing in MRP, DCP, CP and National filing for the EU or Support regulatory submissions publishing for Annual reports, Safety Reports, updates to DMF, labeling, stability and CMC sections for US. Reviews and maintains regulatory database comprising existing and new regulations pertaining to submission requirements for the region. Regular interaction with internal stakeholders and external stakeholders like Local Affiliates/ MC (Marketing Company) through emails & teleconference, through proper communication channels to ensure accuracy and completeness of submission and resolving issues as andwhen they arise. Escalates unresolved issues appropriately as per the agreed escalation process. Ensures that the quality and TAT targets defined are always met.Experience Required: Two or more years of experience in pharmaceutical industry submission publishing or related technical skills Minimum 1-year hands-on experience in working with Documentum and industry leading publishing tools, preferably Liquent Insight Publisher is required Experience with word processing, use/applications of templates, bookmarking, hyper-linking, Microsoft Office applications is required Familiarity with FDA or EU regulations & guidelines is preferred Practical understanding of evolving technologies in support of business area is preferredSkills Required: The candidate should possess strong attention to detail, exhibit excellent interpersonal communications (in English, both verbal & written), organizational, time management and follow-up skills. The candidate must also demonstrate personal initiative, responsibility, flexibility, the ability to work under limited supervision, and be able to handle multiple project assignments Managing own work: ability to prioritize, plan and organize multiple assignments, and to work under strict timelines Global Regulatory Knowledge; familiarity with regulatory resources (i.e., location, interpretation and application of global regulations and guidelines relating to regulatory affairs) Basic understanding of information management concepts and tools needed to support business area. Use various technical skills to resolve publishing/document preparation issues. Ability to demonstrate a solid command of the technical tools at the level required to perform job dutiesTo Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below:a) For Position in Mumbai Search : Job Code # 369b) For Position in Bangalore Search : Job Code # 370c) For Position in Hyderabad Search : Job Code # 371

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 Management b) Hands on experience of Study Conduct and Close Out is must c) Any Graduate To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below:a) For Position in Mumbai Search : Job Code # 95b) For Position in Bangalore Search : Job Code # 98

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 Pune Search : Job Code # 84b) For Position in Nagpur Search : Job Code # 85c) For Position in Bangalore Search : Job Code # 86

HiWe are Hiring for the job role of Medical WriterJob 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 requiredTo 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)

HiWe are hiring for Leading ITES Company for PV Aggregate Reporting Profile.Skillsa) Minimum 2 years of experience in Periodic/Scientific Aggregate Safety Report writingb) Experience is documents i.e., PBRER,PSUR,DSUR, ICH GuidelinesJob ResponsibilityMinimum 2 years of experience in Periodic/Scientific 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 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 years of medical writing work experience including 1 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 skills Qualifications Health Care Professional OR Masters/bachelors degree in Life Sciences/PhysicianTo Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below:a) For Position in Mumbai Search : Job Code # 54b) For Position in Pune Search : Job Code # 55

HiWe are hiring for Leading ITES Company for PV Aggregate Reporting Profile.Skillsa) Minimum 2 years of experience in Periodic/Scientific Aggregate Safety Report writingb) Experience is documents i.e., PBRER,PSUR,DSUR, ICH GuidelinesJob ResponsibilityMinimum 2 years of experience in Periodic/Scientific 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 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 years of medical writing work experience including 1 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 skills Qualifications Health Care Professional OR Masters/bachelors degree in Life Sciences/PhysicianTo Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below:a) For Position in Mumbai Search : Job Code # 54b) For Position in Pune Search : Job Code # 55

Hi, We are hiring for Leading ITES Company for SDTM Programmer Profile.Please go through the JD and we will get back to the relevant profiles.Job Description:Minimum 3 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 deliverablesImplementation 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 & TLFExperience 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 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 Leading ITES Company for PV Aggregate Reporting Profile.Skillsa) Minimum 2 years of experience in Periodic/Scientific Aggregate Safety Report writingb) Experience is documents i.e., PBRER,PSUR,DSUR, ICH Guidelinesb) Qualifications - Health Care Professional OR Masters/bachelors degree in Life Sciences/PhysicianJob ResponsibilityMinimum 2 years of experience in Periodic/Scientific 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 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 years of medical writing work experience including 1 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 skillsQualifications Health Care Professional OR Masters/bachelors degree in Life Sciences/PhysicianTo Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below:a) For Position in Mumbai Search : Job Code # 54b) For Position in Pune Search : Job Code # 55

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 Pune Search : SAS + CDB Programmer Pune (Job Code # 84)b) For Position in Mumbai Search : SAS + CDB Programmer Mumbai (Job Code # 83)

HiWe are Hiring for the job role of Medical WriterJob 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 requiredTo 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 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 clinicaldevelopment 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)

Hi We are Hiring For Leading ITES Company for the position of PV Aggregate Reporting Role Job Description 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 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 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 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 Mumbai Search : Job Code # 373b) For Position in Pune Search : Job Code # 374