{"id":2687762,"url":"https://alion.io/job/elligo-clinical-research-coordinator-ii","title":"Clinical Research Coordinator II","company":{"id":4421812,"name":"Elligo","domain":"elligo.com","url":"https://alion.io/company/elligo","size_band":"201-500","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Paylocity","truth_index":null},"role":"Administrative","role_family":"Administrative","seniority":"middle","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Gilbert, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":44000,"max_usd":83000,"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},{"name":"Microsoft Office","optional":false},{"name":"Outlook","optional":false},{"name":"SharePoint","optional":false}],"status":"live","first_seen_at":"2026-10-02T19:18:31Z","employer_posted_date":"2026-10-16","last_verified_at":"2026-10-23T01:25:20Z","board_verified":true,"closed_at":null,"days_open":20,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":20},"description":"Description\n JOB SUMMARY\n(To perform this job satisfactorily, an individual must be able to perform each essential duty satisfactorily. Other duties may be assigned.)\nThis individual will play a key role in the conduct of clinical trial activities, in accordance with all applicable regulations governing the conduct of clinical trials. The primary skills include logical thinking, the ability to prioritize, a “can-do” attitude, the ability to adapt quickly to changing business conditions, and strong interpersonal and team-building skills.\nThe CRC II will have overall responsibilities for coordinating efforts with other study team members in order to achieve protocol objectives and corporate goals, including:\n ESSENTIAL DUTIES\nDevelop strong working relationships and maintain effective communication with study team members. \nDevelop strong working relationships and become the point of contact for the clinic as well as the sponsor for clinic related activities. \nManage multiple concurrent trials \nAssist with mentoring and training study team members \nComplete all protocol-related training \nPerform patient/research participant scheduling \nCollect patient/research participant history \nCollects and maintains source documentation \nPerforms data entry and query resolution \nCollect and review required essential study documents and reports. Order supportive study supplies (e.g., contracts, IXRS, lab kits, non-clinical supply materials, imaging, and laboratory handling manuals, etc.). \nAdhere to an IRB-approved protocol \nConduct the informed consent process of research subjects. \nSupport the safety of research subjects, report adverse events \nCoordinate protocol-related research procedures, study visits, and follow-up and anticipate and mitigate potential non-compliance \nAssist with the screening, recruiting, and enrollment of research subjects. \nFacilitate pre-study, site qualification, study initiation, monitoring visits, and study close-out activities \nCollect, process, and ship laboratory specimens \nFollow ethical and professional codes of conduct and escalate noncompliance as needed \nCommunicate with Stakeholders: CRAs, Project Managers, Patient Services, Account Managers, healthcare practices \nAdhere to the study plan by ensuring that all approvals are in place, vendors are qualified \nComply with Elligo, Clinic, and Sponsor policies, standard operating procedures (SOPs), GCP guidelines, and documents data according to ALCOA. \nComply with Elligo, Clinic, and Sponsor policies, standard operating procedures (SOPs), and guidelines. \n WORKING CONDITIONS\nThe above statements are intended to describe the general nature and level of work being performed by individuals assigned to this position. They are not intended to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel. More in-depth information can be found in SOP's, working guidelines, policies, etc.\nTraveling CRC II positions will require (50%) travel for this position. Non-traveling will require (15- 25%) travel.\nElligo is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at Elligo are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, national, social or ethnic origin, sex (including pregnancy), age, physical, mental or sensory disability, HIV Status, sexual orientation, gender identity and/or expression, marital, civil union or domestic partnership status, past or present military service, family medical history or genetic information, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. Elligo will not tolerate discrimination or harassment based on any of these characteristics. In addition, Elligo will provide reasonable accommodations for qualified individuals with disabilities.\nRequirements\n KNOWLEDGE SKILLS AND ABILITIES REQUIRED\nMinimum 3 years of experience coordinating clinical trials, including the activities listed above \nBS/BA in Life Science or related discipline or equivalent work experience \nPrevious nursing experience in a clinical setting a plus \nCCRC certification a plus \nDemonstrated ability in positive relationship building, with strong verbal and written skills required. \nKnowledge of clinical trial terminology and practices required \nDemonstrated ability to coordinate complex protocols with overlapping timelines \nPrior GCP training and ability to explain importance of GCP guidelines \nManagement of regulatory documents throughout trial lifecycle \nAbility to train others on key protocol elements and study task execution \nAble to clearly explain and enforce clinical research participant safety requirements including safety reports, ICF elements and role of the IRB \nStrong interpersonal skills with attention to detail a must \nFollow ethical and professional codes of conduct \nTake action to minimize participant risk \nAdhere to the study plan by ensuring that all approvals are in place, vendors are qualified \nComply with Elligo, Clinic, and Sponsor policies, standard operating procedures \n(SOPs), GCP guidelines and documents data according to ALCOA \nDemonstrated proficiency with word processing, spreadsheet, database, and presentation software (MS Office skills such as Outlook, Word, Excel, PowerPoint, and SharePoint) and with clinical trial master filing systems. \nAbility to travel for Clinic activities, and attend investigator meetings or vendor visits/audits, as required. \nStrong organization/prioritization skills for the management of multiple concurrent projects","description_format":"text","description_chars":5751,"description_truncated":false,"requirements":{"experience_years_min":3,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":{"level":"bachelor","optional":true},"security_clearance":false,"languages":[]},"benefits":[],"hiring_locations":[],"hiring_excludes":[],"relocation_offered":false,"industries":[],"lifecycle":[{"event":"open","at":"2026-10-16T08:09:04Z"}],"visa":[],"liveness":{"score":71,"band":"hot","label":"Hiring now","p_open":1,"p_active":0.787,"p_room":0.9,"age_days":19,"expected_fill_days":30,"reasons":["conf:3","win:mid"],"computed_at":"2026-10-22T06:10:10Z"},"pay":null,"html_url":"https://alion.io/job/elligo-clinical-research-coordinator-ii","json_url":"https://alion.io/job/elligo-clinical-research-coordinator-ii.json","meta":{"generated_at":"2026-10-23T03:58:28Z","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":6512,"day_limit":null,"remaining_today":null,"minute_limit":300,"resets_at":"2026-10-24T00:00:00Z"}},"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":4421812},"rest":"https://alion.io/mcp/rest/get_company?id=4421812"},"human":"https://alion.io/catalog?offer=company.slices&for=job%2Felligo-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%2Felligo-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%2Felligo-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/elligo-clinical-research-coordinator-ii\", \"note\": \"what you need it for\"}"},"human":"https://alion.io/catalog?offer=company.verify&for=job%2Felligo-clinical-research-coordinator-ii"}]}