{"id":2687781,"url":"https://alion.io/job/elligo-clinical-research-coordinator-i","title":"Clinical Research Coordinator I","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":"junior","employment_type":null,"work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["El Paso, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":{"min":18,"max":24,"currency":"USD","period":"hour","gross":null,"usd_annual":48000},"salary_estimate":null,"experience_years_min":1,"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},{"name":"Microsoft Teams","optional":true}],"status":"live","first_seen_at":"2026-09-25T16:43:59Z","employer_posted_date":"2026-10-16","last_verified_at":"2026-10-18T21:42:56Z","board_verified":true,"closed_at":null,"days_open":23,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":23},"description":"Description\nSUMMARY:\nThe Clinical Research Coordinator I plays a key role assisting 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. This role works closely with study team members and supports other study team members to achieve study objectives and corporate goals.\n ESSENTIAL DUTIES:\nDevelop strong working relationships and maintain effective communication with study team members. \nBecome the point of contact for the site as well as the sponsor for site related activities. \nManage multiple concurrent trials \nCompletes 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 \nSupport the collection and review of required essential study documents and reports. \nOrder supportive study supplies (e.g., contracts, IXRS, lab kits, nonclinical supply materials, imaging and laboratory handling manuals, etc.). \nAdhere to an IRB approved protocol \nOnce trained, will conduct 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-ups \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 \nFollows ethical and professional codes of conduct \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. \n QUALIFICATIONS:\nAbility to identify and explain key protocol elements and perform study tasks Understanding of basic participant safety requirements including safety reports, ICF elements, and role of the IRB \nStrong interpersonal skills with attention to detail are a must \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 work with functional groups and different levels of employees throughout Elligo to achieve business results effectively and professionally.\nProactive and timely follow-up skills: the ability to organize applicable department timelines and follow up with internal and external stakeholder needs as needed.\nClear and concise written and oral communication skills, including the ability to present ideas and suggestions clearly and effectively.\nStrong organizational skills: ability to accomplish multiple tasks within the agreed-upon timeframes through effective prioritization of duties and functions in a fast-paced environment.\nProven track record of building and maintaining solid relationships with both internal and external stakeholders.\nSelf-motivated; able to work independently to complete tasks respond to department requests and collaborate with others to utilize their resources and knowledge to identify quality solutions.\nCRC Qualifications:\nSkilled in interacting and working with others, including peers, patients, management, and internal and external stakeholders.\nWorking knowledge of Good Clinical Practice guidelines and Federal research regulations.\nFamiliarity in clinical trial terminology and practices required\nThe ability to manage multiple tasks, evaluate a variety of unpredictable scenarios, and achieve project timelines while being able to apply your understanding of study protocol(s).\nStrong computer skills, including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS), and MS Office products such as Excel and Word.\nAn honest and ethical work approach to promote the development of life-changing treatments for patients.\nEDUCATION AND EXPERIENCE:\nAssociates Degree or BS/BA in Life Science or related discipline preferred \nAt least one year of experience in coordinating clinical trials\nPrevious nursing experience in a clinical setting is a plus \nPrior GCP training and ability to explain the importance of GCP guidelines \nENVIRONMENT:\nOn-site\n PHYSICAL DEMANDS:\nWhile performing the duties of this job, the employee may:\nwork at a desk using a computer for prolonged periods;\nregularly communicate via e-mail, telephone, chat, webcam (remote sessions such as MS Teams or Zoom), and exchange accurate and timely information;\nfrequently sit/stand/walk, grasp lightly/fine manipulation of objects\noccasionally reach/work above shoulders, twist/bend/stoop/squat, grasp forcefully, lift/carry/push/pull objects that weigh up to 20 pounds.\n ADDITIONAL:\nElligo Health Research is a dynamic organization in a rapidly changing industry. Accordingly, the responsibilities associated with this job may change from time to time in accordance with business needs. More specifically, the incumbent may be required to perform additional and/or different responsibilities from those set forth above.\nThe above declarations are not intended to be an all-inclusive list of the duties and responsibilities of the job described, nor are they intended to be such a listing of the skills and abilities required to do the job. Rather, they are designed only to describe the general nature of the job.\nThe incumbent must be flexible as there may be workweeks that require more than 40 hours to ensure the positions expectations and responsibilities are met.\nElligo Health Research is committed to a policy of equal employment and will not discriminate against an applicant or associate based on his or her age, sex, sexual orientation, gender identity, race, color, creed, religion, national origin or ancestry, citizenship, marital status, familial status, physical or mental disability, handicap, military or veteran status, genetic information, pregnancy or any other category protected under federal, state or local law, regulation or ordinance.\nRequirements\nAssociates Degree or BS/BA in Life Science or related discipline preferred\nAt least one year of experience in coordinating clinical trials\nPrevious nursing experience in a clinical setting is a plus\nPrior GCP training and ability to explain the importance of GCP guidelines\nSalary Description\n$18.00 - $24.00 per hour","description_format":"text","description_chars":6714,"description_truncated":false,"requirements":{"experience_years_min":1,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":{"level":"associate","optional":true},"security_clearance":false,"languages":[]},"benefits":[],"hiring_locations":[],"hiring_excludes":[],"relocation_offered":false,"industries":["Biotechnology"],"lifecycle":[{"event":"open","at":"2026-10-16T08:09:04Z"}],"visa":[],"liveness":{"score":58,"band":"ok","label":"Likely open","p_open":1,"p_active":0.77,"p_room":0.75,"age_days":21,"expected_fill_days":27,"reasons":["conf:1","win:late","comp:junior"],"computed_at":"2026-10-17T05:46:00Z"},"pay":{"stated_usd_annual":48000,"is_top_pay":false},"html_url":"https://alion.io/job/elligo-clinical-research-coordinator-i","json_url":"https://alion.io/job/elligo-clinical-research-coordinator-i.json","meta":{"generated_at":"2026-10-18T23:37:10Z","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":26184,"day_limit":null,"remaining_today":null,"minute_limit":300,"resets_at":"2026-10-19T00:00:00Z"}},"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-i"},{"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-i"},{"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-i"},{"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-i\", \"note\": \"what you need it for\"}"},"human":"https://alion.io/catalog?offer=company.verify&for=job%2Felligo-clinical-research-coordinator-i"}]}