Veeva CDMS

Job Summary:We are seeking a skilled Veeva CDMS Professional to ensure the seamless operation of our systems.Key Responsibilities:Collaborate with cross-functional teams to resolve complex technical issues.Provide top-notch support to end-users, addressing their concerns effectively.Requirements:Demonstrated experience in Architecture Principle Design,...

Atorus industry-leading clinical trial analytics experts build tools and solutions that efficiently facilitate data management and biometrics activities. We carry this out by automating and applying advancing services and technology to maximize trial efficiency, ease interpretation, and prepare your clinical trial data to quickly deliver actionable...

Hi Hope you are doing well Please look at below mentioned Job Description and share your updated resume and mention your work authorization & Current Location . If the JD match with your skills. Role: IRT TESTER (offshore) Location: India (Remote) Duration: Long Term Contract Job Description: OVERVIEW We are looking for a well-rounded Clinical...

Role : Lead Clinical Database Programmer – CDMExp : 8 to 10 yrsWork Mode : Hybrid / RemoteLooking for Immediate Joiners onlyArea :Study set-up and Migration activities using Rave/Veeva/Oracle Clinical/InformFunction :Clinical data management & DevelopmentSub Function :Development- (eCRF/Edit Checks/custom functions/Clinical Trails/Reports)Responsibilities...

Role : Lead Clinical Database Programmer – CDM Exp : 10 to 13 yrs Work Mode : Hybrid / Remote Looking for Immediate Joiners only Area : Study set-up and Migration activities using Rave/Veeva/Oracle Clinical/Inform Function : Clinical data management & Development Sub Function : Development- (eCRF/Edit Checks/custom functions/Clinical Trails/Reports)...

Role : Lead Clinical Database Programmer – CDMExp : 10 to 13 yrsWork Mode : Hybrid / RemoteLooking for Immediate Joiners onlyArea :Study set-up and Migration activities using Rave/Veeva/Oracle Clinical/InformFunction :Clinical data management & DevelopmentSub Function :Development- (eCRF/Edit Checks/custom functions/Clinical Trails/Reports)Responsibilities...

Role : Lead Clinical Database Programmer – CDMExp : 10 to 13 yrsWork Mode : Hybrid / RemoteLooking for Immediate Joiners onlyArea :Study set-up and Migration activities using Rave/Veeva/Oracle Clinical/InformFunction :Clinical data management & DevelopmentSub Function :Development- (eCRF/Edit Checks/custom functions/Clinical Trails/Reports)Responsibilities...

Role & responsibilitiesVeeva Vault CDMS (Clinical Data Management System)Key Responsibilities:Strong Understanding of Clinical trial processes,GCP,and EDC system workflowsFamiliarity with Vault CDMS architecture, object configuration and User rolesSet up EDC studies in Vault CDMS using Studio.Configure study design elements (forms, edit checks, rules, and...

Atorus industry-leading clinical trial analytics experts build tools and solutions that efficiently facilitate data management and biometrics activities. We carry this out by automating and applying advancing services and technology to maximize trial efficiency, ease interpretation, and prepare your clinical trial data to quickly deliver actionable insights....

Job Title: Clinical Data ManagementLocation: Mumbai & Bangalore or PAN INDIA (WFO)Experience: 810+ years, hands-on in clinical data management-relevant exp should be 5.5 to 7 years exp needed only in current projectSkills:Reva DatabaseVeeva CDMS (Do not source Veeva Vault EDMM)User Acceptance Testing (UAT) on patient data & patient databasesExperience with...

Veeva Vault CDMS (Clinical Data Management System)Key Responsibilities:Strong Understanding of Clinical trail processes,GCP,and EDC system workflowsFamiliarity with Vault CDMS architecture, object configuration and User rolesSet up EDC studies in Vault CDMS using Studio.Configure study design elements (forms, edit checks, rules, and custom...

UAT Tester - CTMS & CDM applicationsKeywords Clinical Systems, Safety Systems, 21 CFR part 11, GAMP 5, ICH, EMEA, MHRA regulationsRoles and ResponsibilitiesMust Have48+ years of experience in IT testing/validation, with 2–4+ years in clinical trial systems.Collaborate with Clinical Operations, Data Management, Biostatistics, and IT teams to gather UAT...

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery,...

Job OverviewZS life science R&D team partners with clients to discover and develop innovative medicines that improve patient lives. Our work spans across consulting, analytics and technology (services and platforms) projects across several domains. We have 3,500+ professionals delivering R&D programs, invested in R&D data, analytics and technology assets,...