Clinical Research Associate I

AbbVie

Gurgaon, India
Not specified
Review and analyze regulatory documents
Maintain clinical trial information systems
Support creation of patient and regulatory binders
AbbVie is seeking a Clinical Research Associate I in Gurgaon, India, to support site management activities, focusing on regulatory document management and collaboration with clinical operations teams. The ideal candidate will have a background in natural sciences or related fields, with strong communication skills and familiarity with clinical trials

Job Summary

  • The Site-ICRA I is primarily responsible for support services in partnership and collaboration with the US and EMEA Clinical Site Operations team.
  • Primary focus is on providing and leading support of site management activities such as collection of essential site regulatory documents by reviewing and analyzing regulatory documents for accuracy and completeness per Good Clinical Practice (GCP) and Good Documentation Practice (GDP) standards.
  • Clinical inventory management with site and local warehouse and liaison between site, global project management, Device Accountability Specialist, local warehouse, and local customer service.

Matching Summary

Match Score: 75

AbbVie is seeking a Clinical Research Associate I in Gurgaon, India, to support site management activities, focusing on regulatory document management and collaboration with clinical operations teams. The ideal candidate will have a background in natural sciences or related fields, with strong communication skills and familiarity with clinical trials.

Skills & Requirements

Must-have

  • Review and analyze regulatory documents
  • Maintain clinical trial information systems
  • Support creation of patient and regulatory binders
  • Communicate and collaborate with all levels
  • Clinical inventory management

Nice-to-have

  • Engage in professional associations
  • Seek continuing education
  • Contribute to process improvements

Key Requirements

  • Bachelor's degree in natural science or equivalent
  • Minimum two years of experience
  • Proficient in Microsoft Office Suite
  • Familiarity with clinical trials research processes

Work Rights

Not specified

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