Clinical Research Associate II

Job Summary

A company is looking for a Clinical Research Associate II and Senior CRA.

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 and Education

• Bachelor's degree in a scientific or healthcare-related field
• Minimum of 2 years of independent monitoring experience
• Experience monitoring complex therapeutic areas like Oncology, Obesity, and/or Gastrointestinal studies preferred
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
• Ability to work independently and collaboratively in a fast-paced environment