{"id":1756844,"url":"https://alion.io/job/evolution-research-group-clinical-research-coordinator","title":"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":11,"ghost_share":0,"stale_share":1,"repost_share":0,"time_to_fill_p50_days":null,"computed_at":"2026-10-10T05:45:15Z"}},"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":["Little Rock, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":{"min":25,"max":30,"currency":"USD","period":"hour","gross":null,"usd_annual":60000},"salary_estimate":null,"experience_years_min":null,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GCP","optional":false}],"status":"live","first_seen_at":"2026-10-02T20:24:00Z","employer_posted_date":"2026-10-02","last_verified_at":"2026-10-11T17:19:06Z","board_verified":true,"closed_at":null,"days_open":9,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":9},"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 include medical and dental coverage, a matching 401(k), and paid time off to recharge.\nJob Description:\nThe Clinical Research Coordinator is responsible for the overall coordination, organization, management, and efficient implementation of clinical trials. The CRC completes all study related procedures and distributes study medication and instructions to research subjects under the direction of the Principal Investigator and the Site Director. They maintain accurate, confidential files and documentation of study participants. In executing these position responsibilities, the Clinical Research Coordinator is guided by FDA regulations, Good Clinical Practice (GCP), and company standard operating procedures and policies.\nResponsibilities:\nGeneral\nObtain detailed knowledge of all components of each study protocol through review and analysis of study information with Principal Investigator and Site Director prior to the effective date of the study.\nAssist to develop draft source documents and review the documents for accuracy and clarity prior to study start up.\nReview with Principal Investigator and Site Director, any components of the study for which additional information or clarification are required prior to the initiation of the study.\nManage studies with direct oversight from Site Director, and Principal Investigator to ensure compliance with protocol requirements.\nManage studies with Principal Investigator, Site Director, and Recruitment Manager to develop effective programs for study enrollment. \nContribute to the SOP review and development as delegated by the Site Director. \nStudy Management\nPerform study activities as delegated by the Principal Investigator and under the supervision of the Site Director.\nAttend the investigator meeting for each assigned protocol, as appropriate with directive from Site Director. \nIn conjunction with Site Director and Principal Investigator, ensure adherence to the protocols and document breaches or violations with sponsors and appropriate Institutional Review Boards (IRBs) and other outside regulatory organizations, as required.\nScreen, enroll subjects and schedule subject visits in conjunction with Principal Investigator\nReview and obtain informed consent from with potential study volunteer\nDocument all written and phone correspondences with sponsor, labs, IRB other regulatory organizations\nMaintain organized, accurate and complete study records\nAssist Principal Investigator in conducting studies in manner to ensure integrity of data and safety of subjects.\nEnter data as appropriate for protocol (paper-electronic data capture)\nIn conjunction with Principal Investigator, accurately report and track adverse events as defined by each study protocol.\nPerform study close-out procedures.\nStore study records appropriately\nAdditionally, this role may encompass responsibilities beyond those outlined above, as required by the evolving needs of the organization. This job description is intended as a foundation and may be subject to expansion or modification to best suit ERG’s objectives.\nSkills and Qualifications:\nEducation and experienceHigh School Diploma or its equivalent; College degree preferred.\nAble to communicate with providers, co-workers, sponsors, and others in a collaborative and courteous manner. \nKnowledgeable in medical terminology to communicate with physician office and laboratory staff. \nDemonstrate the initiative to act independently, initiate activity as required and make appropriate decisions within the constraints of study protocols, regulatory requirements, and company policy.\nAble to initiate or modify behavior to achieve desired outcomes in spite of environmental factors, priorities, or problems that might not be well defined or that are subject to change.\n\n RequirementsUnderstand regulatory requirements, as well as Good Clinical Practices (GCP) and International Conference of Harmonization (ICH) guidelines. \nExcellent communication skills (interpersonal, written, verbal) \nBasic computer skills to include Word, Excel, as well as proprietary applications unique to the clinical research industry (such as Study Manager)","description_format":"text","description_chars":4897,"description_truncated":false,"requirements":{"experience_years_min":null,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":{"level":"high_school","optional":true},"security_clearance":false,"languages":[]},"benefits":[],"hiring_locations":[],"hiring_excludes":[],"relocation_offered":false,"industries":["Biotechnology","Health Care","Clinical Trial Sites & Recruitment"],"lifecycle":[{"event":"open","at":"2026-10-03T11:06:29Z"}],"visa":[],"liveness":{"score":54,"band":"ok","label":"Likely open","p_open":1,"p_active":0.575,"p_room":0.945,"age_days":7,"expected_fill_days":21,"reasons":["conf:3","stale_co","win:mid"],"computed_at":"2026-10-10T05:45:15Z"},"pay":{"stated_usd_annual":60000,"is_top_pay":false},"html_url":"https://alion.io/job/evolution-research-group-clinical-research-coordinator","json_url":"https://alion.io/job/evolution-research-group-clinical-research-coordinator.json","meta":{"generated_at":"2026-10-11T21:20:57Z","cache_seconds":300,"methodology":"https://alion.io/methodology","terms":"https://alion.io/terms","contact":"https://alion.io/contact","api":"https://alion.io/developers","about":"Alion is a live layer of people, companies and AI agents: who they are, whether they are real and active right now, what they do and how to work with them, readable by people and by agents and paid per call.","catalog":"https://alion.io/catalog.json","usage":{"tier":"crawler_verified","counted_by":"address","units_charged":1,"used_today":10170,"day_limit":null,"remaining_today":null,"minute_limit":300,"resets_at":"2026-10-12T00:00:00Z"}},"offers":[{"id":"company.slices","title":"One company in depth, by slice","status":"live","price":{"credits":0.02,"usd":0.002,"plus_per_slice":{"credits":0.05,"usd":0.005}},"unit":"per company, plus each slice with data","note":"the employer in depth","call":{"mcp_tool":"get_company","arguments":{"id":3876300},"rest":"https://alion.io/mcp/rest/get_company?id=3876300"},"human":"https://alion.io/catalog?offer=company.slices&for=job%2Fevolution-research-group-clinical-research-coordinator"},{"id":"market.stats","title":"A market slice: pay, demand and time to fill","status":"live","price":{"credits":1,"usd":0.1},"unit":"per slice","note":"pay, demand and time to fill for this role and place","call":{"mcp_tool":"market_stats"},"human":"https://alion.io/catalog?offer=market.stats&for=job%2Fevolution-research-group-clinical-research-coordinator"},{"id":"job.search","title":"Open jobs by role, technology, place, pay and visa","status":"live","price":{"credits":0.02,"usd":0.002},"unit":"per posting in a list","note":"similar open postings","call":{"mcp_tool":"search_jobs"},"human":"https://alion.io/catalog?offer=job.search&for=job%2Fevolution-research-group-clinical-research-coordinator"},{"id":"company.verify","title":"Is this company real and active right now","status":"pilot","price":null,"unit":"per company","request":{"url":"https://alion.io/catalog/request","method":"POST","body":"{\"offer\": \"company.verify\", \"for\": \"job/evolution-research-group-clinical-research-coordinator\", \"note\": \"what you need it for\"}"},"human":"https://alion.io/catalog?offer=company.verify&for=job%2Fevolution-research-group-clinical-research-coordinator"}]}