Clinical Research Associate Ii

Merck & Co., Inc., Rahway, NJ, USA

São Paulo, Brazil
Hybrid
Ich-gcp compliance
Site management and monitoring
Data integrity and subject safety
Merck & Co., Inc. is seeking a Clinical Research Associate II to support their clinical trials in São Paulo and Porto Alegre, Brazil. The ideal candidate will ensure compliance with research protocols and regulations while maintaining strong relationships with study sites

Job Summary

  • You will be the primary site contact throughout all phases of clinical research studies, ensuring compliance with regulations and contributing to the success of our clinical trials.
  • Conduct remote and on-site monitoring to ensure data integrity and subject safety.
  • Manage information in Clinical Trial Management Systems (CTMS) and electronic Trial Master Files (eTMF).

Matching Summary

Match Score: 85

Merck & Co., Inc. is seeking a Clinical Research Associate II to support their clinical trials in São Paulo and Porto Alegre, Brazil. The ideal candidate will ensure compliance with research protocols and regulations while maintaining strong relationships with study sites.

Skills & Requirements

Must-have

  • ICH-GCP compliance
  • site management and monitoring
  • data integrity and subject safety
  • clinical trial protocols
  • regulatory documentation review
  • Clinical Trial Management Systems

Nice-to-have

  • continuous improvement of processes
  • Subject Matter Expert
  • share best practices and training

Key Requirements

  • Bachelor’s degree
  • Solid experience as a Clinical Research Associate
  • Fluent in local languages and advanced proficiency in English
  • Strong understanding of clinical research processes
  • Proficiency in MS Office and clinical IT applications

Work Rights

Not specified

Tailored Resume

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