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Clinical Research Associate

  1. India
2024-111565
  1. Clinical Monitoring
  2. 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

     

List #1

Day in the life

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How to excel as a CRA in a Clinical Research Organisation

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Our People

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Publish date

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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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Brazil-based CRA II Debora Oh shares her tips on how to become a great CRA and provides insight into life at ICON.

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Progressing as a CRA with ICON

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Publish date

05/23/2023

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How to progress as a Clinical Research AssociateTo thrive as a Clinical Research Associate (CRA), it is imperative to cultivate a multifaceted skill set and demonstrate unwavering commitment to exce

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 Senior CRA Yemi Moses recounts her development and shares her career ambitions with ICON plc.

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From Clinical Trial Assistant to Clinical Operations Manager, Adrienne Purdy shares her journey.Tell us about you role and what you do at ICON?  I have been at ICON since 2013 and I have been growing

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Adrienne Purdy shares her career journey and experience at ICON.

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