Clinical Trial Specialist II

Job Summary

To support clinical trial operations, the full-time remote Clinical Trial Specialist II will manage site recruitment and feasibility, conduct remote monitoring and site management activities, and ensure compliance with regulatory requirements while mentoring junior staff.

Key responsibilities:

• Manage regulatory document submissions and track site compliance with IRB requirements
• Conduct site evaluations, provide training, and maintain site relationships to ensure protocol adherence
• Create and maintain Trial Master Files (TMF) and ensure audit readiness of essential documents

Required qualifications:

• Bachelor's degree or relevant work experience required
• 2+ years of relevant clinical research experience required
• Demonstrated ability to lead and mentor Clinical Trial Specialists
• Proficient in Microsoft Office applications and adaptable to new computer systems
• Basic knowledge of medical terminology is desired