Job Summary

• Perform site activation activities under general supervision, ensuring compliance with applicable regulations, SOPs, project plans, and contractual/budgetary guidelines.
• Track, follow up, and support the approval and execution of regulatory, ethics, ICF, Investigator Pack (IP), and other essential documents.
• Maintain and update internal systems, databases, trackers, timelines, and project plans with accurate site‑specific information.

Matching Summary

Skills & Requirements

Key Requirements

• Bachelor's degree in Life Sciences
• Minimum 1 year experience
• Healthcare or clinical research environment
• General knowledge of clinical trial environment
• Attention to detail
• Organizational and time-management skills
• Manage multiple projects simultaneously
• Interpersonal and communication skills
• Proficiency in MS Office

Work Rights