Senior Clinical Research Associate (argentina)

PFM

Argentina
**
Independently oversees study site management
Conducts on-site and remote monitoring visits
Ensures ich-gcp and local regulatory compliance
** PFM is seeking a Senior Clinical Research Associate (CRA) in Argentina to oversee complex clinical trials, manage site operations, and mentor junior staff. This remote position requires extensive experience in clinical research, with a focus on ensuring data quality and compliance throughout the trial process. **

Job Summary

  • The role involves independently overseeing all aspects of study site management to ensure patient safety and high-quality data generation across Argentina.
  • Incumbents are expected to manage complex clinical trials while supporting Clinical Trial Managers and mentoring junior staff members.
  • The position requires conducting various site visits including pre-study, initiation, routine monitoring, and close-out in accordance with ICH-GCP standards.

Matching Summary

Match Score: 75

** PFM is seeking a Senior Clinical Research Associate (CRA) in Argentina to oversee complex clinical trials, manage site operations, and mentor junior staff. This remote position requires extensive experience in clinical research, with a focus on ensuring data quality and compliance throughout the trial process. **

Skills & Requirements

Must-have

  • Independently oversees study site management
  • Conducts on-site and remote monitoring visits
  • Ensures ICH-GCP and local regulatory compliance
  • Manages site start-up and recruitment procedures
  • Performs Investigator Site File (ISF) reviews

Nice-to-have

  • Experience mentoring junior staff members
  • Ability to negotiate study budgets
  • Strong relationship building with investigators
  • Participation in global clinical meetings
  • Assistance with protocol development review

Key Requirements

  • Wide-ranging experience handling complex assignments
  • Knowledge of ICH-GCP and local regulations
  • Ability to manage appropriately sized or complex clinical trials
  • Experience with audit readiness standards
  • Proficiency in managing Investigator Site Files

Work Rights

Not specified

Tailored Resume

Cover Letter