{"id":1137517,"url":"https://alion.io/job/psi-clinical-research-associate-ii-19","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":"hybrid","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":85000,"max_usd":173000,"period":"year","method":"role_seniority_country_remote_cell","sample_n":100},"experience_years_min":2,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"Microsoft Office","optional":false}],"status":"live","first_seen_at":"2026-09-23T00:37:03Z","employer_posted_date":"2026-10-06","last_verified_at":"2026-10-29T08:47:24Z","board_verified":true,"closed_at":null,"days_open":36,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":36},"description":"PSI is a leading Contract Research Organization with more than 30 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:\nAct as the main line of communication between the project team, sponsor, and the site\nBuild and maintain a good relationship with the site staff involved in the study conduct\nPrepare, conduct, and report site selection, initiation, routine monitoring and close-out visits\nEnsure that subject recruitment targets are timely defined, communicated, recorded and met, and project timelines are followed at site level\nEnsure accurate and timely information flow with trial sites on Adverse Events and protocol/process deviations\nPerform source data verification and follows up on data queries at site level; review and manage study risks on a site level\nEnsure proper handling, use, accountability, reconciliation, and return of all Investigational Product(s) and clinical study supplies on sites\nReview essential study documents and reconcile study Investigator Site File (ISF) / TMF at site level\nEnsures quality (data integrity and compliance) at site level\nConduct site audit preparation visits and resolve site audit findings\nParticipate in study site audits and client onsite visits, as required\nEnsure the flow of documents and study supplies between the project team, site and the Central/ Regional Laboratory/ Central Reviewer/ Warehouse\nConduct project-specific training of site investigators\nSupport preparation of Investigator newsletters\nAssist Site Management Associates in maintaining study-specific and corporate tracking systems at site level\nSupport preparation of draft regulatory and ethics committee submission packages\nSupport collection of IP-RED packages at site/country level\nFacilitate review and reconciliation of the study TMF on country and site levels \n College/University degree in Life Sciences or an equivalent combination of education, training & experience\nLocated in the Central or West Coast regions is preferred\nMust have 2+ years of independent on-site monitoring experience\nExperience in all types of monitoring visits, in phases I-III\nExperience in Oncology mandatory & GI preferred and/or radio-pharm experience preferred.\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 up to 75%\nValid driver’s license (if applicable)\nFor this position PSI is not hiring individuals who require work visa for employment or continued employment now or anytime in the future.\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.\nFor this position, PSI is not 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