Clinical Research Associate
- India
- Clinical Monitoring
- ICON Strategic Solutions
TA Business Partner
- Icon Strategic Solutions
About the role
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As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Responsibilities:
- On-Site monitoring
- IRB Submission
- Management of the responsible sites
- Direct site communication
- Managing different stakeholders and vendors
Qualification:
- Education: B.Pharm/M.Pharm/Pharm D/BDS/MBBS
- minimum 1 year of onsite monitoring (excluding any training & induction) of respiratory/cardiology/nephrology studies
- Strong & clear communication skills
Location: Mumbai & Delhi location
A better career. A better world. A better you.
Our people are our greatest strength, are the core of our culture and the driving force behind our success. Throughout all levels of the company, our people have a drive to succeed and a passion that ensures what we do, we do well. We help you build exciting and rewarding careers, deliver results to help bring life-changing medicine and devices to market and maintain ICON’s success as an industry leader. See all locations Read more
Day in the life
Teaser label
Our PeopleContent type
BlogsPublish date
08/29/2023
Summary
To excel as a Clinical Research Associate (CRA) in a Clinical Research Organization (CRO), you need a combination of education, skills, and the right mindset. Brazil-based CRA II Debora shares her
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