{"id":1621640,"url":"https://alion.io/job/panoramic-clinical-research-coordinator-ii","title":"Clinical Research Coordinator II","company":{"id":34511,"name":"Panoramic","domain":"panoramic.city","url":"https://alion.io/company/panoramic","size_band":"501-1000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Dayforce","truth_index":{"grade":"B","score":75,"open_postings":5,"ghost_share":0,"stale_share":1,"repost_share":0,"time_to_fill_p50_days":27,"computed_at":"2026-10-20T05:45:00Z"}},"role":"Administrative","role_family":"Administrative","seniority":"middle","employment_type":null,"work_mode":"on_site","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":49000,"max_usd":92000,"period":"year","method":"role_seniority_country_remote_cell","sample_n":1977},"experience_years_min":3,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GCP","optional":false}],"status":"live","first_seen_at":"2026-09-30T05:00:00Z","employer_posted_date":"2026-10-01","last_verified_at":"2026-10-20T10:17:57Z","board_verified":true,"closed_at":null,"days_open":20,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":20},"description":"Clinical Research Coordinator II\nLake Michigan Nephrology | St. Joseph, MI\n\nLake Michigan Nephrology is seeking an experienced Clinical Research Coordinator II (CRC II) to lead clinical research activities at our St. Joseph, Michigan site. This role is responsible for supporting the successful execution of clinical trials from recruitment and enrollment through study completion while ensuring patient safety, data quality, protocol compliance, and adherence to Good Clinical Practice (GCP).\n\nThe CRC II will work closely with Principal Investigators, physicians, clinic staff, patients, sponsors, and centralized research teams to build effective recruitment and enrollment workflows and ensure high-quality study execution. This is an excellent opportunity for a research professional who enjoys working directly with patients and providers and wants to make an impact within a growing nephrology research program.\n\nWhat You’ll Do\nLead day-to-day clinical research activities at the site level across assigned clinical trials.\nRead, understand, and implement study protocols, including eligibility criteria, visit schedules, procedures, and data collection requirements.\nPrescreen patients and proactively identify potential research participants through collaboration with physicians and clinic staff.\nDevelop and implement effective workflows to support patient recruitment, referral, informed consent, enrollment, and retention.\nPartner with the Central Enrollment Team and other research departments to achieve referral, consent, and enrollment goals.\nObtain and document informed consent in accordance with ICH/GCP, protocol requirements, and site SOPs.\nTrain site staff on study objectives, procedures, and requirements and maintain appropriate training documentation.\nEvaluate site resources and coordinate with clinic leadership to ensure appropriate space, equipment, supplies, and staffing are available.\nCoordinate and conduct protocol-specific patient visits while maintaining compliance with visit windows and study requirements.\nPerform clinical procedures including vital signs, height/weight measurements, blood collection, specimen processing, and ECGs as required by protocol.\nCollect, process, and ship laboratory specimens according to protocol and applicable requirements.\nDispense, collect, and maintain accurate accountability records for investigational products/study medications when applicable.\nComplete case report forms (CRFs), patient tracking tools, and other study documentation accurately and within required timelines.\nMaintain organized and audit-ready source documentation and study files.\nPrepare for monitoring visits by ensuring source documents, logs, accountability records, and other required materials are current and readily available.\nRespond promptly to monitor findings and ensure outstanding items and queries are appropriately resolved.\nReport Adverse Events and Serious Adverse Events to the appropriate IRB, sponsor, and management in accordance with reporting requirements.\nMaintain accurate, timely, and high-quality data in accordance with ALCOA principles.\nMaintain a thorough understanding of study-specific data collection instruments and ensure data is collected according to protocol.\nSupport compliance with GCP, IATA, FDA regulations, institutional SOPs, and study-specific requirements.\nManage multiple studies and a high volume of research patients while maintaining attention to detail and patient safety.\nPerform other duties and responsibilities as assigned.\n\nWhat We’re Looking For\n3–5+ years of clinical research experience\nBachelor’s degree in a health-related field preferred.\nMedical Assistant (MA) certification preferred.\nGCP and/or IATA certification preferred.\nACRP or SOCRA certification preferred.\nBilingual English/Spanish skills preferred.\nExperience in CKD, nephrology, vascular access, or a related therapeutic area is a plus.\nStrong knowledge of medical terminology and clinical research practices.\nHands-on experience with basic clinical procedures, including blood draws, vital signs, height/weight, and ECGs.\nStrong understanding of Good Clinical Practice (GCP) and applicable FDA and IATA requirements.\nExcellent interpersonal and communication skills with the ability to work effectively with patients, physicians, clinic staff, sponsors, and research teams.\nHighly organized, self-motivated, and detail-oriented with the ability to independently drive study activities and enrollment goals.\nAbility to manage competing priorities and multiple clinical trials in a fast-paced environment.\nStrong commitment to patient safety, data integrity, protocol compliance, and timely study execution.\nFlexibility to work a schedule that supports patient visits and study requirements.\n\nWhy Join Lake Michigan Nephrology?\nAt Lake Michigan Nephrology, you’ll have the opportunity to contribute to clinical research that advances treatment options and improves care for patients living with kidney disease. As a site-level research leader, you’ll have meaningful interaction with patients and providers while playing a key role in the successful delivery of clinical trials.","description_format":"text","description_chars":5152,"description_truncated":false,"requirements":{"experience_years_min":3,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":null,"security_clearance":false,"languages":[{"language":"Spanish","level":"Proficiency (C2)","optional":true},{"language":"English","level":"Proficiency (C2)","optional":false}]},"benefits":[],"hiring_locations":[],"hiring_excludes":[],"relocation_offered":false,"industries":[],"lifecycle":[{"event":"open","at":"2026-10-01T20:47:46Z"}],"visa":[],"liveness":{"score":60,"band":"ok","label":"Likely open","p_open":1,"p_active":0.8,"p_room":0.75,"age_days":20,"expected_fill_days":27,"reasons":["conf:0","win:late"],"computed_at":"2026-10-20T05:45:00Z"},"pay":null,"html_url":"https://alion.io/job/panoramic-clinical-research-coordinator-ii","json_url":"https://alion.io/job/panoramic-clinical-research-coordinator-ii.json","meta":{"generated_at":"2026-10-20T11:47:36Z","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":13024,"day_limit":null,"remaining_today":null,"minute_limit":300,"resets_at":"2026-10-21T00:00:00Z"}},"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":34511},"rest":"https://alion.io/mcp/rest/get_company?id=34511"},"human":"https://alion.io/catalog?offer=company.slices&for=job%2Fpanoramic-clinical-research-coordinator-ii"},{"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%2Fpanoramic-clinical-research-coordinator-ii"},{"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%2Fpanoramic-clinical-research-coordinator-ii"},{"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/panoramic-clinical-research-coordinator-ii\", \"note\": \"what you need it for\"}"},"human":"https://alion.io/catalog?offer=company.verify&for=job%2Fpanoramic-clinical-research-coordinator-ii"}]}