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PSI CRO AG

Clinical Research Associate II

PSI CRO AG

. Conduct and report all types of onsite monitoring visits .

Posted 9/17/2026full-timeRemote • Saint-Maur-des-Fossés • FranceJuniorMid-LevelWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in conducting onsite monitoring visits and managing site communications while ensuring compliance with regulatory standards. Proficient in clinical study processes across various therapeutic areas, with strong problem-solving and collaboration skills.

Highest-signal resume keywords
On-Site Monitoring ExperiencePhase II/III MonitoringOncology ExperienceFull Working Proficiency in EnglishMS Office Proficiency

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
CRF ReviewSource Document VerificationQuery ResolutionStudy StartupFeasibility Research
Soft Skills
Communication SkillsCollaboration SkillsProblem-Solving SkillsAbility to MultitaskTeam Environment Adaptability
Industry Keywords
Life SciencesClinical StudiesTherapeutic IndicationsRegulatory SubmissionsMonitoring Visits

About the role

Key responsibilities & impact
  • 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
  • Serve as a point of contact for in-house support services and vendors
  • Communicate with internal project teams regarding study progress
  • Participate in feasibility research
  • Support the regulatory team in preparing documents for study submissions
  • Work on clinical studies across different therapeutic indications while maintaining high quality standards

Requirements

What you’ll need
  • College/University degree in Life Sciences or an equivalent combination of education, training & experience
  • Independent on-site monitoring experience in France
  • Experience in all types of monitoring visits in Phase II and/or III
  • Experience in oncology, hemophilia, infectious diseases, GI
  • Full working proficiency in English
  • 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
  • CV/resume must be submitted in English

Benefits

Comp & perks
  • Big professional advancement opportunity within Clinical Operations with specific mentorship and training program
  • Development opportunities across PSI departments
  • Flexible working hours
  • Home-office option available
  • Combination of home and office work arrangement
  • Extensive onboarding trainings and professional development training programs
  • Highly developed company culture and positive team atmosphere
  • Additional leave days (12 days of RTT)