Research Analyst

• Manage site start-up activities from feasibility and qualification through site activation
• Build working relationships with investigators and site staff as the primary contact for assigned sites
• Prepare, review, negotiate, and execute regulatory and site documents, including confidentiality disclosure agreements, informed consent forms, translations, and amendments
• Coordinate submissions and approvals with Institutional Review Boards, Independent Ethics Committees, Ministries of Health, and Regulatory Authorities
• Develop and track site activation strategies, timelines, and regulatory plans
• Maintain accurate, high-quality documentation in clinical trial management, electronic trial master file, and trial master file systems
• Identify, resolve, or escalate site issues and risks related to activation, recruitment, compliance, training, and data quality
• Support sites with study system access, training requirements, and readiness activities
• Ensure assigned sites remain audit-ready and inspection-ready throughout the study lifecycle
• Maintain compliance with Good Clinical Practice guidelines, local regulations, sponsor requirements, and Parexel standard operating procedures
• Collaborate across functions to achieve project milestones and deliverables, communicating progress, risks, and issues

Explore Research Associate, ICRA at Parexel. Review requirements and application details.

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