Site Activation Specialist I

Job Summary

Responsible for start‑up of investigative sites in all phases of clinical trials. Primarily oversees site contracts, ethics and regulatory submissions, essential document collection, and site activation activities, ensuring local activities meet timelines, budgets, and quality standards. Acts as primary contact with Regulatory Authorities and Ethics Committees under guidance of project leads.

Job Responsibilities

• Provide quality deliverables at the country level, following project requirements and applicable country rules, under oversight of the SSU Country Manager.
• Adhere to forecasted submission/approval timelines, track milestones in the SSU tracking system, provide rationale for delays, and plan contingencies.
• Monitor financial aspects of the project, including hours/tasks per contract, and report discrepancies.
• Review and comply with SOPs and Work Instructions, maintain tr...