{"id":1756859,"url":"https://alion.io/job/evolution-research-group-assistant-clinical-research-coordinator","title":"Assistant Clinical Research Coordinator","company":{"id":3876300,"name":"Evolution Research Group","domain":"ergclinical.com","url":"https://alion.io/company/evolution-research-group","size_band":null,"is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"ADP","truth_index":{"grade":"B","score":75,"open_postings":12,"ghost_share":0,"stale_share":1,"repost_share":0,"time_to_fill_p50_days":null,"computed_at":"2026-10-13T05:45:00Z"}},"role":"Administrative","role_family":"Administrative","seniority":null,"employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Miami, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":{"min":22,"max":27,"currency":"USD","period":"hour","gross":null,"usd_annual":54000},"salary_estimate":null,"experience_years_min":null,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GCP","optional":false},{"name":"HIPAA","optional":false}],"status":"live","first_seen_at":"2026-09-02T17:59:00Z","employer_posted_date":"2026-09-02","last_verified_at":"2026-10-12T18:00:00Z","board_verified":true,"closed_at":null,"days_open":40,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":40},"description":"About Company:\nEvolution Research Group (ERG) is dedicated to delivering high-quality Phase I-IV clinical trial execution to help sponsors bring lifesaving and life-enhancing therapies to market quickly and safely. Founded in 2014, ERG has grown into a leading neuroscience clinical development company, with affiliate sites across the U.S.and deep expertise in clinical pharmacology, psychiatry, neurology, acute pain, and metabolic disorders. ERG has completed over 5,000 trials and continues to expand into high-need therapeutic areas in the U.S. and globally.\nWhy join us? We offer a supportive culture, meaningful work, and the opportunity to contribute to cutting-edge research alongside industry leaders. Plus, we offer competitive benefits includemedical and dental coverage, a matching 401(k), and paid time off to recharge.\n\nJob Description:\nERG is the largest independent clinical research site services company focused on special populations and is the market leader in CNS. With 18 wholly owned clinical sites, we conduct in-patient and out-patient phase I-IV clinical research studies. Our mission is to provide the highest quality execution of clinical trials in all clinical research phases aimed at helping sponsor companies to get their life saving or life enhancing drugs to market as quickly and safely as possible.\nThe Assistant Coordinator participates in clinical research studies conducted by the Clinical Research Coordinator. They assist and perform a variety of duties involved in the collection, compilation, documentation and analysis of clinical research data.\nResponsibilities:\nAdministrative:\nMonitor and ensure study data is collected following plan of care, guidelines and identified group resources\nServe in rotation with assistant clinical coordinators and clinical research coordinators\nServe as liaison between assigned clinical research coordinator and all clinical departments \nParticipate in collaborative team efforts with other departments\nDiscuss and administer Informed Consent Form\nCheck and ensure that procedure areas are properly stocked with study supplies and equipment (i.e. blood tubes, kits, study flowsheets, ECG machines, BP cuffs, etc.)\nAssist assigned Clinical Research Coordinator review study schedules to ensure that study procedures are properly staffed\nAssist assigned Clinical Research Coordinator with the creation and/or review of study flowsheets to ensure study is conducted according to protocol requirements \nAnticipate, recognize, and resolve issues\nReads and understands each protocol in which she/he is involve\nFollow established guidelines in the collection of clinical data and/or administration of clinical studies\nPerforms all other duties as assigned\nClinical Responsibilities\nSupport adverse event reporting and informed consent administration\nNotify staff of abnormal results or incidents\nEnsure participant comfort and readiness for procedures\nSet up supplies and procedure areas per protocol\nPerform venipuncture, vital signs, ECG, and other assessments\nCommunicate with participants to explain procedures and gather data\nAssist with patient care and emergency measures as needed\nAttend study initiation meetings and perform study-related tasks\nProvide high-quality care under pressure\nEducational:\nMaintains current licensure, registration and/or certification within educational background\nMaintains current BLS and/or ACLS certification\nMaintains necessary CEU’s for licensure, registration and/or certification\nActively participates on CPMI’s ongoing Quality Assurance Program, HIPAA and Compliance Programs\nKeeps apprised of all new OSHA and GCP/ICH rules and regulations\nAttends all appropriate team meetings regarding study protocols\nMaintains skills in use of EKG machines, Holter hook-up and monitoring, diabetic monitoring and taking accurate vital signs\nReads and understands CPMI policy and procedures manuals, SOP manual and employee handbook","description_format":"text","description_chars":3937,"description_truncated":false,"requirements":{"experience_years_min":null,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":null,"security_clearance":false,"languages":[]},"benefits":[],"hiring_locations":[],"hiring_excludes":[],"relocation_offered":false,"industries":["Biotechnology","Health Care","Clinical Trial Sites & 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