Site Activation Specialist
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Job Summary
To support clinical research studies, the full-time Site Activation Specialist will manage site activation and maintenance activities remotely, ensuring timely completion of start-up tasks and compliance with regulatory requirements.
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 related 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 with Microsoft Office applications and contemporary digital systems
Complete Job Description
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