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The Clinical Data Engineer 1 works with close supervision to support various activities related to electronic data, and/or the application of computer and communication technologies. General areas of ...
pythonsqldata warehousingtrend analysiscustomer focuscustom reportsinformaticaroot cause21 cfrjavalife cycleproject teamsclinical dataglobal teamsHey Guys! Great new to all clinical Sas programmers,We have huge openings in our top MNC client, 1. 8 to 10 years of experience in programming related activities for clinical studies (Phase I to IV...
statsdtmlistingssas programmingsurvival analysissasdata managementopeningsbase sasstatistical reportingmathematicsspecificationspredictive modelingclinicalstatistical programmingstatisticsreportinglogistic regressionichgcpHey Guys! Great new to all clinical Sas programmers,We have huge openings in our top MNC client, 1. 8 to 10 years of experience in programming related activities for clinical studies (Phase I to IV...
statsdtmlistingssas programmingsurvival analysissasdata managementopeningsbase sasstatistical reportingmathematicsspecificationspredictive modelingclinicalstatistical programmingstatisticsreportinglogistic regressionichgcpThe Senior Database Programmer provides technical expertise for the conduct of clinical trials, might act as an internal subject matter expert in specific areas providing technical support and expert ...
21 cfrtechnical supportdatabase designdata managementclinical researchsoftware development life cyclelife cycleclinical trialsclinical data managementsoftware developmentquality standardsThe Senior Database Programmer provides technical expertise for the conduct of clinical trials, might act as an internal subject matter expert in specific areas providing technical support and expert ...
21 cfrtechnical supportdatabase designdata managementclinical researchsoftware development life cyclelife cycleclinical trialsclinical data managementsoftware developmentquality standardsThe Senior Database Programmer provides technical expertise for the conduct of clinical trials, might act as an internal subject matter expert in specific areas providing technical support and expert ...
clinical data managementprogrammingbiomedicalcrfdatabase designdata managementclinical trialstechnical supportquality standardsedcecrfdesigntrialssciencedatabaseclinicaladditionichgcpEnsure compliance with SOPs/Guidelines, ICH-GCP, and any other applicable local and international regulations, and participate in internal/external audits and regulatory inspections as required. Proa...
data managementregulatorywork effectivelyinternational regulationscfr21 cfrsas programmingreportingsasregulatory requirementscompliancesdtmichgcpUse efficient programming techniques to produce/QC derived datasets (e.g. SDTM, ADaM), tables, figures, and data listings. Produce/QC dataset specifications and other process supporting documents and...
compliancecfrquality controlgcpwork effectivelycontrolbusiness21 cfrproject managementquality managementmetricstime managementsdtmadamfigurescustomer focusprogrammingquality standardsichgcpUse efficient programming techniques to produce/QC derived datasets (e.g. SDTM, ADaM), tables, figures, and data listings. Produce/QC dataset specifications and other process supporting documents and...
compliancecfrquality controlgcpwork effectivelycontrolbusiness21 cfrproject managementquality managementmetricstime managementsdtmadamfigurescustomer focusprogrammingquality standardsichgcpUse efficient programming techniques to produce/QC derived datasets (e.g. SDTM, ADaM), tables, figures, and data listings. Produce/QC dataset specifications and other process supporting documents and...
compliancecfrquality controlgcpwork effectivelycontrolbusiness21 cfrproject managementquality managementmetricstime managementsdtmadamfigurescustomer focusprogrammingquality standardsichgcpUse efficient programming techniques to produce/QC derived datasets (e.g. SDTM, ADaM), tables, figures, and data listings. Produce/QC dataset specifications and other process supporting documents and...
compliancecfrquality controlgcpwork effectivelycontrolbusiness21 cfrproject managementquality managementmetricstime managementsdtmadamfigurescustomer focusprogrammingquality standardsichgcpUse efficient programming techniques to produce/QC derived datasets (e.g. SDTM, ADaM), tables, figures, and data listings. Produce/QC dataset specifications and other process supporting documents and...
compliancecfrquality controlgcpwork effectivelycontrolbusiness21 cfrproject managementquality managementmetricstime managementsdtmadamfigurescustomer focusprogrammingquality standardsichgcpThe Clinical Data Analyst I (CDA I) shall perform all clinical data cleaning activities on assigned projects, commensurate with experience and/or project role. Further responsibilities shall include s...
data managementcrfdata entryquality controlvalidationdata analysisclinical datadata cleaningdata processingdata validationdatabase programmingbusinessanalysisdatabaseclinicalprotocolichgcpSALARY: Upto 6 LPA QUALIFICATION: Bsc/BE-Chemical MALE/FEMALE: Both EXPERIENCE: 3 years to 4 years JOB DETAILS 1)Needs to en...
safety case dataentry continuousimprovementfacilitation drugsafety clinical benefits marketing operations healthcare ContinuousImprovementCulture Kaizen RootCauseAnalysis 5S SixSigma da medical ichgcpGood knowledge of ICH-GCP guidelines and applicable regulatory requirements. Well versed with handling TMF and other trial related activities to support the study teams as per the scope of SLA service...
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