Vacancy description

Senior CRA in Bangalore, भारत

ICON

  • On-siteWork from the office

Bangalore, भारत

ICON seeks a Senior Clinical Research Associate to oversee clinical trial monitoring and site management in India. The role requires ensuring protocol adherence, regulatory compliance, and data integrity while leading a team of clinical research professionals across multiple trial sites.

Responsibilities

  • Monitor clinical trial sites for adherence to protocols, regulatory requirements, and GCP standards
  • Conduct site visits to assess performance, identify issues, and provide operational support
  • Collaborate with cross-functional teams on timely data collection and accurate reporting
  • Train and guide site staff and other CRAs on clinical trial conduct standards
  • Build and maintain effective relationships with site personnel and stakeholders

Requirements

  • Bachelor's degree in relevant scientific or healthcare field
  • Minimum 6 years experience as Clinical Research Associate in onsite monitoring
  • Demonstrated experience with oncology trials
  • Strong knowledge of clinical trial processes and regulatory requirements including GCP standards
  • Proficiency with clinical trial software and monitoring tools
  • Ability to manage multiple sites and projects with strong organizational skills
  • Willingness to travel approximately 60% as required

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