Clinical Research Associate 2 - Based in Portugal
IQVIA · Lisbon, Portugal
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
IQVIA seeks a Clinical Research Associate 2 based in Lisbon to conduct site monitoring and regulatory oversight for clinical trials. The role involves site visits, subject recruitment support, quality evaluation, and cross-functional collaboration with study sites and clients.
What they're looking for
- University degree in scientific or healthcare discipline
- 2-4 years independent on-site monitoring experience
- Fluent in Portuguese and English
- Proficient with MS Office and computer systems
- Strong organizational and problem-solving abilities
- Valid class B driver's license
- Willingness to travel frequently
What you'll be doing
- Conduct site selection, initiation, monitoring, and close-out visits
- Support development and execution of subject recruitment strategies
- Evaluate site compliance with Good Clinical Practice and ICH guidelines
- Track regulatory submissions, enrollment metrics, case report forms, and data queries
- Communicate with site staff and client representatives to resolve operational issues
Privacy & handoff
This role links to IQVIA's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.