Site Activation Specialist

Job Summary

To support clinical research studies, the full-time remote Site Activation Specialist will coordinate site regulatory documentation, ensure timely completion of activation milestones, and facilitate site feasibility activities while collaborating with cross-functional teams.

Key responsibilities

• Coordinate the collection, tracking, review, and maintenance of site regulatory and essential documents
• Partner with study teams and sites to ensure timely completion of start-up activities and activation milestones
• Review study-specific regulatory documentation, identify gaps, and drive corrective actions prior to final approval

Required qualifications

• Bachelor's degree in a relevant scientific discipline with at least one year of clinical research experience
• Previous experience in the pharmaceutical, biotechnology, or CRO industry
• Working knowledge of ICH GCP and relevant clinical research regulations
• Strong understanding of clinical research processes and regulatory documentation requirements
• Proficiency in Microsoft Word, Excel, PowerPoint, and other digital systems