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Associate Manager - Clinical Operations #clinicalresearch #clinicaltrials #medicine #research #healthcare #medicalresearch #clinicaltrial #science #clinical #health #clinicalstudies #pharma #medical #pharmacy #biotech #covid #biopharma #pharmaceuticals #clinicalstudy #pharmacovigilance #medicalaffairs #clinicalresearchassociate #pharmaindustry #doctor #pharmaceuticalindustry #phd #oncology #dru
The Associate Management Service Delivery is responsible for the day-to-day management and supervision of a Clinical Data Management team to ensure the successful implementation of the global data transmission strategy, structures, processes, and metrics in order to deliver outstanding customer satisfaction People Responsibilities: Supervise the day-to-day operations of the team members including
Back End Developer #backenddeveloper #frontenddeveloper #programming #fullstackdeveloper #webdeveloper #developer #javascript #html #coding #css #softwaredeveloper #programmer #python #webdevelopment #reactjs #java #coder #developerlife #code #javascriptdeveloper #developers #backend #webdevelopers #computerscience #codingmemes #frontend #androiddeveloper #programmingmemes #php #programmers und
Business Analyst #businessanalyst #businessanalysis #business #agile #projectmanagement #businessanalytics #productmanagement #iiba #technology #dataanalytics #datascience #elearning #innovation #businesstips #training #ba #dataanalyst #businessowner #businessanalysts #certification #agiledevelopment #scrum #projectmanager #softwaredevelopment #cbap #productdevelopment #dataanalysis #businessat
Central Monitor (Analytics) #clinicalresearch #clinicaltrials #clinicaldataanalyst #REGULATORYaffairs #medicalcoding #medicalbilling #research #healthcare #medicalresearch #clinicaltrial #science #clinical #health #clinicalstudies #pharma #medical #pharmacy #biotech #clinicareers #pharmacovigilance #pharmaceuticals #clinicalstudy #pharmacovigilance #medicalaffairs #clinicalresearchassociate #ph
Centralized Study Specialist I #clinicalresearch #clinicaltrials #clinicaldataanalyst #REGULATORYaffairs #medicalcoding #medicalbilling #research #healthcare #medicalresearch #clinicaltrial #science #clinical #health #clinicalstudies #pharma #medical #pharmacy #biotech #clinicareers #pharmacovigilance #pharmaceuticals #clinicalstudy #pharmacovigilance #medicalaffairs #clinicalresearchassociate
Management of projects under direction of a Project Manager / Director as assigned. Ensure site monitoring responsibility for clinical studies are conducted according to Standard Operating Procedures, ICH Guidelines and GCP. Work Closely with project teams in implementation of best TRR practices & applicable project plans as assigned (Implementation of Initiatives either independently or with t
Management of projects under direction of a Project Manager / Director as assigned. Ensure site monitoring responsibility for clinical studies are conducted according to Standard Operating Procedures, ICH Guidelines and GCP. Work Closely with project teams in implementation of best TRR practices amp; applicable project plans as assigned Implementation of Initiatives either independently or with tea
Clinical Data Analyst #clinicalresearch #clinicaltrials #clinicaldataanalyst #REGULATORYaffairs #medicalcoding #medicalbilling #research #healthcare #medicalresearch #clinicaltrial #science #clinical #health #clinicalstudies #pharma #medical #pharmacy #biotech #clinicareers #pharmacovigilance #pharmaceuticals #clinicalstudy #pharmacovigilance #medicalaffairs #clinicalresearchassociate #pharmain
Perform all data management tasks as appropriate to include, but not to be limited to data review and query management to ensure that quality standards both internal and client are achieved. Assist with review clinical trial data in accordance with Data Management Plans, Edit Check Specifications and/or Data Review Guidelines and raise queries to resolve erroneous, missing, incomplete data. Generat
Perform all data management tasks as appropriate to include, but not to be limited to data review and query management to ensure that quality standards (both internal and client) are achieved. Assist with review clinical trial data in accordance with Data Management Plans, Edit Check Specifications and/or Data Review Guidelines and raise queries to resolve erroneous, missing, incomplete data. Gener
Clinical Data Coordinator s #clinicalresearch #clinicaltrials #clinicaldataanalyst #REGULATORYaffairs #medicalcoding #medicalbilling #research #healthcare #medicalresearch #clinicaltrial #science #clinical #health #clinicalstudies #pharma #medical #pharmacy #biotech #clinicareers #pharmacovigilance #pharmaceuticals #clinicalstudy #pharmacovigilance #medicalaffairs #clinicalresearchassociate #ph
Clinical Data Coordinator s #clinicalresearch #clinicaltrials #clinicaldataanalyst #REGULATORYaffairs #medicalcoding #medicalbilling #research #healthcare #medicalresearch #clinicaltrial #science #clinical #health #clinicalstudies #pharma #medical #pharmacy #biotech #clinicareers #pharmacovigilance #pharmaceuticals #clinicalstudy #pharmacovigilance #medicalaffairs #clinicalresearchassociate #p
Clinical Data Specialist #clinicalresearch #clinicaltrials #clinicaldataanalyst #REGULATORYaffairs #medicalcoding #medicalbilling #research #healthcare #medicalresearch #clinicaltrial #science #clinical #health #clinicalstudies #pharma #medical #pharmacy #biotech #clinicareers #pharmacovigilance #pharmaceuticals #clinicalstudy #pharmacovigilance #medicalaffairs #clinicalresearchassociate #pharm
Assist with review of clinical trial data in accordance with Data Management Plans and/or Data Review Guidelines and raise queries to resolve erroneous, missing, incomplete data. Demonstrates capability to read and follow study timelines for on-time deliverables and potential to assist with inputs on study design or capable to make suggestions to study timelines when warranted. Run and execute addi
Review clinical trial data in accordance with Data Management Plans and applicable standardized data management processes SOPs; Work Instructions, etc. to identify erroneous, missing, incomplete, or implausible data.Run ancillary programs e.g., diagnostics, special listings, reconciliation discrepancy listings used to support the review of clinical trial data.Generate, resolve and track queries to
Clinical Project Coordinator #clinicalresearch #clinicaltrials #clinicaldataanalyst #REGULATORYaffairs #medicalcoding #medicalbilling #research #healthcare #medicalresearch #clinicaltrial #science #clinical #health #clinicalstudies #pharma #medical #pharmacy #biotech #clinicareers #pharmacovigilance #pharmaceuticals #clinicalstudy #pharmacovigilance #medicalaffairs #clinicalresearchassociate #p
Clinical Project Coordinator #clinicalresearch #clinicaltrials #clinicaldataanalyst #REGULATORYaffairs #medicalcoding #medicalbilling #research #healthcare #medicalresearch #clinicaltrial #science #clinical #health #clinicalstudies #pharma #medical #pharmacy #biotech #clinicareers #pharmacovigilance #pharmaceuticals #clinicalstudy #pharmacovigilance #medicalaffairs #clinicalresearchassociate #
¨ Follow applicable departmental Standard Operating Procedures and Work Instructions. ¨ Complete required trainings according to required timelines. ¨ Complete day-to-day tasks ensuring quality and productivity. ¨ Maintain project and technical documentation in an appropriate manner. ¨ Perform checks to ensure quality of work completed. ¨ Ensure timely escalation as needed. ¨ Other duties as assign
? Follow applicable departmental Standard Operating Procedures and Work Instructions. ? Complete required trainings according to required timelines. ? Complete day-to-day tasks ensuring quality and productivity. ? Maintain project and technical documentation in an appropriate manner. ? Perform checks to ensure quality of work completed. ? Ensure timely escalation as needed. ? Other duties as assign