Clinical Research Associate II

PSI CRO AG

Clinical Research Associate managing onsite monitoring visits across Portugal for clinical studies. Collaborating with internal teams and supporting regulatory processes.

Posted 6/17/2026full-timeRemote • 🇵🇹 PortugalJuniorMid-LevelWebsite

About the role

Key responsibilities & impact

Conduct and report all types of onsite monitoring visits across sites in Portugal
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

What you’ll need

College/University degree in Life Sciences or an equivalent combination of education, training & experience.
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

Comp & perks

Extensive training programs
Profound therapeutic area trainings
Monitors training program
Mentorship programs
Interactive soft-skills trainings

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

on-site monitoringCRF reviewsource document verificationquery resolutionstudy startupregulatory document preparationauditsinspectionsOncologyHematology

Soft Skills

communicationcollaborationproblem-solvingplanningmultitaskingteamwork

Certifications

College/University degree in Life Sciences