Senior Clinical Research Associate

Job Summary

A company is looking for a Senior Clinical Research Associate responsible for monitoring clinical trials and ensuring compliance with regulatory standards.

Key Responsibilities

• Conduct site monitoring visits and ensure adherence to Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• Manage the progress of assigned studies, including tracking regulatory submissions, recruitment, and data management
• Mentor clinical staff and collaborate with study team members for project execution support

Required Qualifications

• Bachelor's Degree in a scientific discipline or health care preferred
• At least 4 years of on-site monitoring experience
• In-depth knowledge of clinical research regulatory requirements, including GCP and ICH guidelines
• Proficiency in Microsoft Word, Excel, and PowerPoint
• Strong therapeutic and protocol knowledge as provided in company training