Senior Clinical Research Associate
PSI CRO AG
full-time
Posted on:
Location Type: Remote
Location: Remote • 🇨🇦 Canada
Visit company websiteJob Level
Senior
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
- Supervise study activities, timelines, and schedules on the country level
- Be a point of contact for in-house support services and vendors
- Be involved in quality control, such as compliance monitoring and reports review
- Participate in feasibility research
- Support regulatory team in preparing documents for study submissions
Requirements
- College/University degree in Life Sciences or an equivalent combination of education, training & experience
- Independent on-site monitoring experience
- Experience in all types of monitoring visits in Phase II and/or III
- Participation in clinical projects as a Lead/Senior Monitor
- Experience in Oncology
- Full working proficiency in English and French
- Proficiency in MS Office applications
- Ability to plan, multitask and work in a dynamic team environment
- Communication, collaboration, and problem-solving skills
- Ability to travel
- Valid driver’s license (if applicable)
Benefits
- Professional development opportunities
- Health insurance benefits
- Flexible work arrangements
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
on-site monitoringCRF reviewsource document verificationquery resolutioncompliance monitoringregulatory document preparationfeasibility researchclinical project managementexperience in OncologyPhase II monitoring
Soft skills
communicationcollaborationproblem-solvingplanningmultitaskingteamworkindependencesupervisiontime managementadaptability