We are currently hiring for Bristol Myers Squibb for Document Coordinator role Looking young professionals with 3 to 5 years of experience in site monitoring, Inform consent form (ICF) with region and different therapeutic areas like Oncology, Immunology, Hematology etc.
Experience Requirements: -
- Startup experience in Country/ site ICF across region like APAC, US & Europe.
- Startup experience in Clinical Trail Package/Essential Document Package/Green light pack approval across region like APAC, US & Europe.
- Seasoned field clinical research associate (Monitor) with min 3+ years of Global Site Monitoring report review experience is preferred with therapeutic area expertise ( Oncology, Cardiology, Hematology, Immunology etc) is preferred.
Location: Hyderabad (Hybrid, 2 Days in a week)
If you are interested with this opportunity share your updated resume to Kusum.kushwaha@iqvia.com
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