{"id":662783,"url":"https://alion.io/job/roviaclinical-clinical-research-coordinator","title":"Clinical Research Coordinator","company":{"id":684736,"name":"Rovia Clinical Research","domain":"roviaclinical.com","url":"https://alion.io/company/roviaclinical","size_band":"51-200","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Rippling","truth_index":null},"role":"Administrative","role_family":"Administrative","seniority":"junior","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Lake City, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":37000,"max_usd":65000,"period":"year","method":"role_seniority_country_remote_cell","sample_n":4386},"experience_years_min":2,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GCP","optional":false},{"name":"Microsoft Office","optional":false}],"status":"live","first_seen_at":"2026-07-29T19:31:53Z","employer_posted_date":"2026-07-29","last_verified_at":"2026-11-10T22:42:44Z","board_verified":true,"closed_at":null,"days_open":104,"trust":{"level":"stale","repost_count":1,"flags":["stale"],"days_open":103},"description":"About Us\nAt Rovia Clinical Research, we’re on a mission to bring innovative treatments to patients, improving the health and lives of our local patient communities. We believe in building a workplace where people feel supported, valued, and excited to grow their careers. Whether you’re just starting out or looking for a new path, you’ll be part of a team that truly works together and makes an impact. Our team is driven by our core values: People First, Humility, Integrity, One Team, and Results Accountability.\nPosition Summary:\nThe Clinical Research Coordinator is responsible for managing and executing clinical trials in accordance with study protocols, ICH/GCP guidelines, sponsor requirements, and Rovia SOPs. This role partners closely with site teams to support study startup, enrollment, data quality, and overall study success.\nKey Responsibilities:\nConducts and coordinates patient visits in accordance with study protocols.\nPerforms clinical tasks such as vital signs, EKGs, specimen collection and processing, and phlebotomy as applicable.\nEnsures informed consent is properly obtained and documented.\nEducates and guides participants through the study, ensuring a positive patient experience.\nMonitors subject safety, reports adverse events, and escalates concerns as appropriate.\nCompletes timely and accurate source documentation and EDC data entry.\nResolves data queries and ensures data integrity.\nMaintains investigational product accountability and proper storage and handling.\nPrepares for and supports monitoring visits, audits, and inspections.\nCollaborates with site staff and investigators to ensure protocol adherence and efficient visit flow.\nPerform other duties as assigned.\nSkills/Abilities:\nStrong knowledge of medical terminology and clinical procedures.\nUnderstanding of ICH/GCP and regulatory requirements.\nExcellent organizational skills and attention to detail.\nStrong interpersonal and patient-facing communication skills.\nAbility to multitask and manage competing priorities in a fast-paced environment.\nProficiency in Microsoft Office, EDC, and CTMS applications.\nAbility to work both independently and collaboratively.\nHigh level of professionalism and commitment to patient confidentiality.\nEducation/Experience:\nHigh school diploma required, bachelor’s degree in related field preferred.\n2+ years of clinical research experience.\nExperience with patient-facing activities (phlebotomy, vital signs, EKGs, etc.) or ophthalmology tasks (OCT imaging, measuring IOP, etc.) strongly 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