Sr Cra 1

IQVIA Inc

São Paulo, Brazil
**
Perform site monitoring visits
Manage study progress
Evaluate site quality and integrity
** IQVIA is seeking a Senior Clinical Research Associate (CRA) to perform monitoring and site management for clinical studies in São Paulo, Brazil. The role requires a minimum of four years of on-site monitoring experience and knowledge of clinical research regulations, particularly in oncology studies. **

Job Summary

  • Perform monitoring and site management work to ensure sites conduct studies and report data as required by the protocol, regulations, and sponsor requirements.
  • Manage the progress of assigned studies by tracking regulatory submissions, recruitment, CRF completion, and data query resolution.
  • Evaluate the quality and integrity of study site practices related to protocol conduct and adherence to regulations.

Matching Summary

Match Score: 75

** IQVIA is seeking a Senior Clinical Research Associate (CRA) to perform monitoring and site management for clinical studies in São Paulo, Brazil. The role requires a minimum of four years of on-site monitoring experience and knowledge of clinical research regulations, particularly in oncology studies. **

Skills & Requirements

Must-have

  • Perform site monitoring visits
  • Manage study progress
  • Evaluate site quality and integrity
  • Maintain Trial Master File (TMF)
  • Adhere to GCP and ICH guidelines

Nice-to-have

  • Drive subject recruitment plans
  • Support project execution
  • Effective time and financial management

Key Requirements

  • At least 4 years of on-site monitoring experience
  • Bachelor's Degree in scientific discipline or health care preferred
  • Good knowledge of clinical research regulatory requirements
  • Good therapeutic and protocol knowledge
  • Proficiency in Microsoft Office Suite
  • Good command of English language

Work Rights

Not specified

Tailored Resume

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