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With over 400 active trials in 5 hub countries, Novartis GDO Trial Management is committed to delivering end-to-end support to make the clinical trial process more efficient and patient-friendly. We b...
powerpoint documentation customerrelations quality delivery goodclinicalpractice documentmanagementsystem trongAt AstraZeneca, we turn ideas into life changing medicines. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. Making the impossible a realit...
siteselection sitemonitoring projectmanagement ocalStudyManagerExperience 0 to 1 year & Freshers can Apply Skills required- CRA knowledge, CRC knowledge, Patient Data knowledge, ICH - GCP, ICF, Adverse Events/ SAEs, site monitoring, remote site monitoring knowle...
clinicaltrials datacollection clinicalresearchassociates clinicalresearch ich-gcpguidelines clinicalpractices rugtrialExperience 0 to 1 year & Freshers can Apply Skills required- CRA knowledge, CRC knowledge, Patient Data knowledge, ICH - GCP, ICF, Adverse Events/ SAEs, site monitoring, remote site monitoring knowle...
clinicalpractices clinicalresearch ich-gcpguidelines clinicalresearchassociates datacollection clinicaltrials rugtrialA career at our company is an ongoing journey of discovery: our around 56,000 people are shaping how the world lives, works and plays through next generation advancements in healthcare, life science a...
it infrastructurebasis customer relationsdata analytics accountsresearch xmlreportingEstablishing and maintaining the Trial Master File (eTMF) together with the trial team and/or the CRO To ensure quality and completeness of the eTMF Performing quality control of the final eTMF and en...
musicmaking qualitycontrol technicalrequirements clinicaltrial bpo css cro ites pharma control clinical archiving healthcare biotechnology etmf PWS Deliverables SourceSelection CPSR tatementsofworksowThis role will be part of DevOps designed Platform team responsible to manage and maintain the Veeva Clinical Vault (VCV) as a Core Platform within Perform Clinical Business Capability supporting miss...
user acceptance testingapplication lifecycle management unit testingtest scripts test metricslife sciences testing toolsagile teEstablishing and maintaining the Trial Master File (eTMF) together with the trial team and/or the CRO To ensure quality and completeness of the eTMF Performing quality control of the final eTMF and en...
musicmaking qualitycontrol technicalrequirements clinicaltrial bpo css cro ites pharma control clinical archiving healthcare biotechnology etmf PWS Deliverables SourceSelection CPSR tatementsofworksowThe TMF Specialist is responsible for Scanning, uploading, Indexing and reviewing documents filed in the eTMF. TMF Spcialist is responsible for verify eTMF Inspection Readiness to ensure clinical tria...
market business argetachievement meetingdeadlines competitive marketcommThis requisition is for 5 Full Time Employees to work as a Hadoop experts CDR, ETMF, AI platform starting from Jan 2019. If not fullfilled data life cycle management will not be complete and will crea...
platforms hadoop ife dataquality datadomain bigdataSet-up, maintain and/or close out project files and study information ((e.g., regulatory documents, Trial Master File (TMF), enrollment, Adverse Events (AEs)/Serious Adverse Events (SAEs), site suppli...
approvalsaes tmfresearch managementregulatory setoperations assurancedatabasesPosition Summary : To become familiar with Trail Master file documentation and Tmf Operations activities in support of client services contracts and internal Icon business needs in accordance with cl...
linical research coordinatordocuments associateclinical research associatePosition Summary : To become familiar with Trail Master file documentation and Tmf Operations activities in support of client services contracts and internal Icon business needs in accordance with cl...
clinical research coordinatordocuments associateclinical research associate© 2019 Hireejobs All Rights Reserved