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IQVIA Inc

Buenos Aires, Argentina
**
Perform site monitoring visits
Administer protocol and study training
Evaluate study site quality
** IQVIA Inc is seeking a Clinical Research Associate (CRA) for a position focused on site monitoring and management across clinical trials in Buenos Aires, Sao Paulo, or Mexico City. The role requires a background in clinical research, a degree in a scientific discipline, and a willingness to travel extensively. **

Job Summary

  • Perform monitoring and site management work to ensure sites are conducting studies and reporting data as required by the study protocol, applicable regulations, and sponsor requirements.
  • Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations, escalating quality issues as appropriate.
  • Create and maintain appropriate documentation regarding site management, monitoring visit findings, and action plans by submitting regular visit reports and generating follow-up letters.

Matching Summary

Match Score: 75

** IQVIA Inc is seeking a Clinical Research Associate (CRA) for a position focused on site monitoring and management across clinical trials in Buenos Aires, Sao Paulo, or Mexico City. The role requires a background in clinical research, a degree in a scientific discipline, and a willingness to travel extensively. **

Skills & Requirements

Must-have

  • Perform site monitoring visits
  • Administer protocol and study training
  • Evaluate study site quality
  • Manage study progress
  • Maintain Trial Master File
  • Create study documentation

Nice-to-have

  • Adapt and drive subject recruitment
  • Support project execution
  • Effective time management skills
  • Establish effective working relationships

Key Requirements

  • 6 months - 4 years on-site monitoring experience
  • Bachelor's Degree in scientific discipline or health care
  • Availability to travel: 80%
  • Written and verbal communication skills
  • Good command of English language
  • Good knowledge of clinical research regulatory requirements
  • Proficiency in Microsoft Word, Excel and PowerPoint

Work Rights

Not specified

Tailored Resume

Cover Letter