Site Activation Partner for Studies

Lead site activation efforts with precision as a Site Activation Partner. Ensure compliance with study timelines and clinical regulations, while managing critical documentation and site issues.
In this role, you will oversee operational activities from study start-up to close-out, focusing on high-quality Investigator Initiation Packages and effective issue resolution. Your experience in clinical trials, regulatory collaboration, and performance tracking will be key in this position. This role requires effective coordination among various support roles to ensure timely site activation.
Key Responsibilities:
• Coordinate Investigator Initiation Package management for site approval
• Support issue resolution and escalate site concerns
• Manage operations for timely activation of clinical sites
• Collaborate with regulatory groups for required submissions
• Update and maintain clinical trial compliance systems
Requirements:
• Bachelor’s degree in life sciences p...