Perform site activation activities under general supervision, ensuring compliance with applicable regulations, SOPs, project plans, and contractual/budgetary guidelines
Job Summary
Perform site activation activities under general supervision, ensuring compliance with applicable regulations, SOPs, project plans, and contractual/budgetary guidelines.
Maintain and update internal systems, databases, trackers, timelines, and project plans with accurate site-specific information.
This is an excellent opportunity for a detail-oriented professional looking to grow within clinical research and site activation functions.
Matching Summary
Perform site activation activities under general supervision, ensuring compliance with applicable regulations, SOPs, project plans, and contractual/budgetary guidelines.
Skills & Requirements
Must-have
Site activation activities
Regulatory and contractual documents
Essential document tracking
Internal systems and databases
Communication of milestones
Nice-to-have
Patient health focus
Innovation and new technologies
Collaboration with stakeholders
Detail-oriented professional
Key Requirements
Bachelor's degree in Life Sciences or related field
Minimum 1 year healthcare/clinical research experience