Covance Hiring for Central Monitor II at Bangalore

Covance Hiring for Central Monitor II at Bangalore #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 #pharmaindustry #doctor #phd #oncology #drugdevelopment #cra #biotechnology # Job Overview: Review Request For Proposal (RFP) opportunities and project/study status for accuracy Running reports of RFPs May support manager and CTMO in preparation of detailed study risk assessment and may coordinate Site Risk Assessment activities. Ensures Critical Data & Process Definition is completed with Data Management and input from project team and ensures implementation of critical data focused EDC design. May populate the RBM tools with the baseline site risk profile. May collate RBM requirements including prescriptive risk factor mitigation strategies, Source Data Verification (SDV)/Source Data Review (SDR) strategy, study-specific risk factor definition, operational risk factor trigger levels. May edit the RBM and Central Monitoring plans in line with emerging risk profile and study changes. Write scripts for User Acceptance Testing and perform UAT for study specific