Clinical Trial Specialist

Job Summary

A company is looking for a Clinical Trial Specialist to oversee site management activities for clinical trials.

Key Responsibilities

• Oversee day-to-day site management activities ensuring compliance with study protocols and regulatory requirements
• Collaborate with site staff and cross-functional teams to resolve issues and ensure timely data collection
• Assist with site initiation, monitoring visits, and close-out activities while providing guidance to junior staff

Required Qualifications

• Bachelor's degree in life sciences, clinical research, or a related field
• Extensive experience in site management, clinical operations, or monitoring within the clinical research industry
• Strong understanding of clinical trial processes, Good Clinical Practice (GCP), and regulatory requirements
• Ability to manage multiple sites and timelines effectively
• Experience in preparing and maintaining site management documentation