{"id":3366036,"url":"https://alion.io/job/psi-clinical-research-associate-ii-28","title":"Clinical Research Associate II","company":{"id":4862,"name":"PSI","domain":"psi-cro.com","url":"https://alion.io/company/psi-cro","size_band":"501-1000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"SmartRecruiters","truth_index":{"grade":"B","score":80,"open_postings":14,"ghost_share":0,"stale_share":1,"repost_share":0,"time_to_fill_p50_days":20,"computed_at":"2026-10-29T05:49:05Z"}},"role":"Biotech","role_family":"Biotech","seniority":"middle","employment_type":"full_time","work_mode":"remote","remote_scope":"stated_countries","remote_scope_basis":"board_field","remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["France"],"countries":["FR"],"hiring_countries":["FR"],"hiring_countries_total":1,"salary":null,"salary_estimate":{"min_usd":41000,"max_usd":99000,"period":"year","method":"global_role_cell_scaled_by_country","sample_n":136},"experience_years_min":null,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"Microsoft Office","optional":false}],"status":"live","first_seen_at":"2026-10-26T10:39:14Z","employer_posted_date":"2026-10-26","last_verified_at":"2026-10-29T17:50:48Z","board_verified":true,"closed_at":null,"days_open":3,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":3},"description":"PSI is a leading Contract Research Organization with more than 22 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.\n As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.\nYou will:\nConduct and report all types of onsite monitoring visits\nBe involved in study startup\nPerform CRF review, source document verification and query resolution\nBe responsible for site communication and management\nBe a point of contact for in-house support services and vendors\nCommunicate with internal project teams regarding study progress\nParticipate in feasibility research\nSupport regulatory team in preparing documents for study submissions\n College/University degree in Life Sciences or an equivalent combination of education, training & experience\nIndependent on-site monitoring experience in France\nExperience in all types of monitoring visits in Phase II and/or III\nExperience in oncology, hemophilia, infectious diseases, GI\nFull working proficiency in English \nProficiency in MS Office applications\nAbility to plan, multitask and work in a dynamic team environment\nCommunication, collaboration, and problem-solving skills\nAbility to travel\n Your CV/resume must be submitted in English\n This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.\nWe offer:\nBig professional advancement opportunity within Clinical Operations with specific mentorship and training program\nDevelopment opportunities across PSI departments\nFlexible working hours\nHome-office option available, as well as combination of home and office work arrangement\nExtensive onboarding trainings and professional development training programs\nHighly developed company culture and positive team atmosphere\nAdditional leave days (12 days of RTT)\n Please submit your CV/resume in 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