Job Summary

• Under general supervision, perform tasks at a country level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines.
• Review documents for completeness, consistency and accuracy, under guidance of senior staff.
• Support the updating and maintenance of internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information.

Matching Summary

Skills & Requirements

Key Requirements

• Bachelor's Degree Life sciences or a related field
• 1-2 years' experience in a healthcare environment or 3 years administrative tasks
• Conversational English
• Good interpersonal communication and organizational skills
• Good word processing skills and knowledge of MS Office applications
• General awareness clinical trial environment and drug development process

Work Rights