Site Activation Coordinator, Spain
Core
Oversee the development, review, and rollout of Informed Consent Forms across multiple countries and studies to ensure patient access to safe treatments.
Role type
Site Activation Coordinator (Clinical Research Operations)
Builds
Regulatory and contractual documents for clinical study sites
Domain
Clinical research / Life sciences
Deliverable
client delivery
Required skills
Regulatory document preparation, ICH/GCP knowledge, Project tracking, Cross-functional partnership, Data accuracy
Preferred skills
Site Activation Specialist experience, Multi-project management
Responsibilities
Prepare and review site regulatory documents for completeness and accuracy; Distribute completed documents to sites and internal teams; Track and follow up on the approval and execution of regulatory, ethics, and Investigator Pack release documents; Update internal systems and project plans with accurate information.
