CRA II

ICON · Bangalore, India

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Clinical OperationsFull-timeCompany career page

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Role summary

Clinical Research Associate II will oversee site qualification, initiation, monitoring, and closeout activities for clinical trials. Responsibilities include ensuring protocol compliance, data integrity, and patient safety, while collaborating with investigators and maintaining high-quality clinical documentation. Requires a bachelor's degree in a science or healthcare field, minimum 3 years of CRA experience, expertise in oncology/immunology/gastroenterology/pulmonology, and willingness to travel 60% domestically and internationally.

What they're looking for

Bachelor's degree in scientific or healthcare-related field
Minimum 3 years experience as Clinical Research Associate with on-site monitoring
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
Current or prior experience in Oncology, Immunology, Gastroenterology, or Pulmonology
Strong organizational and communication skills with attention to detail
Ability to travel 60% of time domestically and internationally with valid driver's license
Legal right to work in India

What you'll be doing

Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
Ensure protocol compliance, data integrity, and patient safety throughout trial process
Collaborate with investigators and site staff to facilitate smooth study conduct
Review data and resolve queries to maintain high-quality clinical data
Prepare and review study documentation including protocols and clinical study reports

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Date posted30 days ago

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