Clinical Research Associate II
PSI CRO AG
full-time
Posted on:
Location Type: Remote
Location: Portugal
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About the role
- 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 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
- Extensive training programs
- Profound therapeutic area trainings
- Monitors training program
- Mentorship programs
- Interactive soft-skills trainings
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
on-site monitoringCRF reviewsource document verificationquery resolutionstudy startupregulatory document preparationauditsinspectionsOncologyHematology
Soft Skills
communicationcollaborationproblem-solvingplanningmultitaskingteamwork