Texas Licensed Senior Clinical Research Associate

Job Summary

A company is looking for a Senior Clinical Research Associate to conduct and monitor clinical trials.

Key Responsibilities

• Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
• Ensure protocol compliance, data integrity, and patient safety throughout the trial process
• Collaborate with investigators and site staff to facilitate smooth study conduct

Required Qualifications

• Bachelor's degree in a scientific or healthcare-related field highly preferred
• Minimum of 2 years of experience as a Clinical Research Associate with on-site monitoring experience
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
• Ability to work independently and collaboratively in a fast-paced environment