Key skills
CommunicationCollaboration
About this role
Role Overview
- Conduct and report all types of onsite monitoring visits
- Be involved in study startup
- Perform CRF review, source document verification and query resolution
- Be responsible for site communication and management
- Be a point of contact for in-house support services and vendors
- Communicate with internal project teams regarding study progress
- Be involved in site identification process
- Support regulatory team in preparing documents for study submissions
- Prepare for and participate in audits and inspections
Requirements
- College/University degree in Life Sciences or equivalent
- At least 2 years of independent on-site monitoring experience in Portugal
- Experience in Oncology, Hematology is a plus
- Full working proficiency in Portuguese, English and MS Office applications
- Ability to plan, multitask and work in a dynamic team environment
- Communication, collaboration, and problem-solving skills
- Ability to travel and valid driver’s license
Benefits
- Extensive training programs
- Profound therapeutic area trainings
- Monitors training program
- Mentorship programs
- Interactive soft-skills trainings