Clinical Research Associate

Job Summary

A company is looking for a FSP CRA (Level I/II).

Key Responsibilities

• Monitor investigator sites using a risk-based approach and ensure compliance with protocols
• Conduct on-site and remote monitoring activities, including data accuracy assessments and documentation of observations
• Facilitate communication between investigative sites, clients, and internal teams while managing administrative tasks

Required Qualifications, Training, and Education

• Strong background in HSA and IRB submissions
• Knowledge of ICH-GCP regulations and compliance requirements
• Experience in conducting on-site file reviews and trial status tracking
• Ability to maintain accurate study systems and documentation
• Familiarity with project publications and process improvement initiatives