{"id":3181919,"url":"https://alion.io/job/care-access-data-coordinator","title":"Data Coordinator","company":{"id":19845,"name":"Care Access","domain":"careaccess.com","url":"https://alion.io/company/care","size_band":"501-1000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Greenhouse","truth_index":{"grade":"B","score":78,"open_postings":3,"ghost_share":0,"stale_share":0.667,"repost_share":0.333,"time_to_fill_p50_days":51,"computed_at":"2026-11-03T05:54:40Z"}},"role":"Administrative","role_family":"Administrative","seniority":"junior","employment_type":null,"work_mode":"remote","remote_scope":"stated_countries","remote_scope_basis":"posting_text","remote_working_hours":null,"hiring_geo_confidence":"inferred","locations":["United States"],"countries":["US"],"hiring_countries":["US"],"hiring_countries_total":1,"salary":{"min":26,"max":36,"currency":"USD","period":"hour","gross":null,"usd_annual":72000},"salary_estimate":null,"experience_years_min":2,"visa_sponsorship":true,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GCP","optional":false}],"status":"live","first_seen_at":"2026-10-23T20:02:05Z","employer_posted_date":"2026-10-23","last_verified_at":"2026-11-03T06:55:52Z","board_verified":true,"closed_at":null,"days_open":10,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":10},"description":"About Care Access\nCare Access is working to make the future of health better for all. With hundreds of research locations, mobile clinics, and clinicians across the globe, we bring world-class research and health services directly to communities that often face barriers to care. We are dedicated to ensuring that every person has the opportunity to understand their health, access the care they need, and contribute to the medical breakthroughs of tomorrow.\nWith programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Through partnerships, technology, and perseverance, we are reimagining how clinical research and health services reach the world. Together, we are building a future of health that is better and more accessible for all.\nTo learn more about Care Access, visit www.CareAccess.com.\nHow This Role Makes a Difference\nData Coordinators play an important role in clinical research by helping ensure study data is accurate, complete, and available when needed. As part of a centralized data coordination team, this role helps protect data integrity, and support Care Access’ mission to make clinical trials more accessible to participants everywhere. \nThrough source data quality control, accurate EDC/CRF transcription, visit-to-entry reconciliation, and proactive query follow-up, Data Coordinators help keep study records reliable and inspection-ready. By catching discrepancies early and helping move issues to resolution, this role contributes to smooth study operations across the Care Access site network. \nHow You'll Make An Impact\nSite-Level Quality Control: Review source data collected during clinic visits and work with clinical staff to clarify or resolve discrepancies before information is entered into Sponsor EDC/CRF systems. Responsibilities include: Reviewing source records for completeness, internal consistency, and required good documentation practices. \nIdentifying missing data, incomplete fields, missing signatures, or other potential documentation issues. \nReviewing source records for consistency with protocol requirements and study workflows. \nDocumenting quality control activities in the approved Care Access system and tracking items through to resolution. \n\nData Reconciliation: Reconcile study data against supporting documentation to make sure required source records are available, complete, and aligned with study expectations. Responsibilities include: Confirming availability of required source materials, including lab reports, ECGs, imaging reports, and other visit-related records. \nReconciling visit documentation against required study data points and expected source records. \nMaintaining and reconciling adverse event information, informed consent logs, protocol deviation logs, and other study tracking tools. \nIdentifying missing or inconsistent documentation and tracking items through to completion or resolution. \n\nEDC/CRF Data Entry: Enter study data into Sponsor EDC/CRF systems accurately and on time, using source documentation and study guidance to support reliable trial records. Responsibilities include: Entering clinical research data in accordance with study requirements, Sponsor expectations, and applicable completion guidelines. \nCompleting data entry within required study timelines and operational expectations. \nVerifying entered data against applicable source documentation before submission or completion. \nApplying study-specific EDC/CRF instructions consistently across assigned studies and visits. \n\nQuery Management: Manage EDC queries and monitor follow-up items by reviewing, routing, responding, and escalating items as needed to keep data issues moving toward closure. Responsibilities include: Reviewing EDC queries generated by Sponsors, CROs, monitors, and EDC systems. \nResolving queries directly when responses are supported by existing source documentation. \nRouting queries that require source clarification, clinical interpretation, investigator assessment, or input from additional site team members. \nEntering approved query responses into the EDC and monitoring open or ageing queries through resolution. \nFollowing up with site personnel when additional input is required and escalating unresolved queries in a timely manner. \nReviewing monitor follow-up letter items and coordinating with site staff, where required, to support timely resolution. \nReporting monitor follow-up items as quality issues in the Care Access QMS, as applicable. \n\nStudy and Site Coordination: Work with study teams and site personnel to keep data workflows organized, address open items, and maintain alignment with protocol and Sponsor expectations. Responsibilities include: Maintaining awareness of assigned study protocols, study-specific requirements, and data entry expectations. \nPrioritizing workload based on participant visits, Sponsor timelines, monitoring visits, and database milestones. \nCommunicating with CRCs, PIs, and site network leadership regarding outstanding data requirements and documentation needs. \nParticipating in study-specific meetings and trainings, as required, to support successful study execution. \n\nOther Responsibilities:Support additional data quality, reporting, documentation, and process improvement work as assigned. \nMaintain study trackers, data logs, dashboards, and other tools used to monitor progress, data completeness, and open action items. \nCollaborate with cross-functional partners during study start-up, maintenance, monitoring, closeout, and audit or inspection readiness activities, as applicable. \n\nThe Expertise Required\nStrong attention to detail and ability to review clinical research documentation for completeness, consistency, and data quality. \nWorking knowledge of clinical trial data workflows, source documentation, EDC/CRF systems, and query management processes. \nAbility to interpret and follow study protocols, completion guidelines, standard operating procedures, work instructions, and study-specific requirements. \nEffective organizational and time management skills, including the ability to prioritize work across multiple studies, visits, deadlines, and competing data needs. \nClear written and verbal communication skills, including the ability to follow up on open items and work effectively with site teams, study teams, monitors, Sponsors, and cross-functional partners. \nAbility to spot data discrepancies, documentation gaps, and recurring quality issues, and raise or help resolve them appropriately. \nComfort working independently in a remote setting while staying accurate, productive, and responsive. \nProficiency with common office and productivity tools, including spreadsheets, shared trackers, email, collaboration platforms, and study related systems. \nCommitment to confidentiality, appropriate handling of clinical research information, and adherence to applicable quality and compliance expectations. \nCertifications/Licenses, Education, and Experience\nMinimum Education:Minimum high school diploma or GED required; associate degree or bachelor’s degree in life sciences, healthcare, clinical research, data management, or a related field preferred. \n\nMinimum Experience:2+ years experience in clinical research, clinical trial support, healthcare operations, data coordination, data entry, quality control, or a related role preferred. \nExperience reviewing, entering, reconciling, or maintaining structured data using electronic systems, spreadsheets, trackers, or databases. \nExperience working with confidential or regulated information and an understanding of the importance of accuracy, documentation quality, and proper information handling. \nFamiliarity with electronic data capture systems, case report forms, clinical source documentation, query resolution preferred. \nExperience working with internal teams, site staff, monitors, Sponsors, CROs, or other cross-functional partners to resolve documentation, data, or operational follow-up items preferred. \nGCP, clinical research, healthcare, or data management experience preferred, but not essential. \n\nHow We Work Together\nLocation: Remote within the United States. This role requires 100% of work to be performed in a remote office environment.\nTravel: This is a remote position with less than 10% travel requirements. Occasional planned travel may be required as part of the role.\nPhysical demands associated with this position Include: The ability to use keyboards and other computer equipment.\nThe expected pay range for this role is $26.00 - $36.00 USD per hour for full time team members.\nBenefits & Perks (US Full Time Employees)\nPaid Time Off (PTO) and Company Paid Holidays\n100% Employer paid medical, dental, and vision insurance plan options\nHealth Savings Account and Flexible Spending Accounts\nBi-weekly HSA employer contribution\nCompany paid Short-Term Disability and Long-Term Disability\n401(k) Retirement Plan, with Company Match \nMandatory Employer Disclosures\nNotice to Illinois applicants: Applicants are not obligated to disclose expunged juvenile records or adjudication, arrest, or conviction.\nNotice to Connecticut applicants: Care Access may require applicants to submit to a urinalysis drug test in connection with an application for employment.\nNotice to Arizona, Georgia, Indiana, and North Dakota applicants: Care Access complies with applicable laws prohibiting smoking in and around places of employment.\nNotice to Massachusetts applicants: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.\nNotice to Rhode Island applicants: Care Access complies with Rhode Island law prohibiting smoking in enclosed areas within places of employment. Care Access is also subject to is subject to Chapters 29-38 of Title 28 of the Rhode Island General Laws.\nNotice to Maryland applicants: UNDER MARYLAND LAW, AN EMPLOYER MAY NOT REQUIRE OR DEMAND, AS A CONDITION OF EMPLOYMENT, PROSPECTIVE EMPLOYMENT, OR CONTINUED EMPLOYMENT, THAT AN INDIVIDUAL SUBMIT TO OR TAKE A LIE DETECTOR OR SIMILAR TEST. AN EMPLOYER WHO VIOLATES THIS LAW IS GUILTY OF A MISDEMEANOR AND SUBJECT TO A FINE NOT EXCEEDING $100. \nDiversity & Inclusion\nWe work with and serve people from diverse cultures and communities around the world. We are stronger and better when we build a team representing the communities we support. We maintain an inclusive culture where people from a broad range of backgrounds feel valued and respected as they contribute to our mission. \nWe are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to, and will not be discriminated against on the basis of, race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.\nCare Access is unable to sponsor work visas at this time.\nIf you need an accommodation to apply for a role with Care Access, please reach out to: ","description_format":"text","description_chars":11392,"description_truncated":false,"requirements":{"experience_years_min":2,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":{"level":"high_school","optional":false},"security_clearance":false,"languages":[]},"benefits":["Retirement plans","Vision insurance"],"hiring_locations":[{"name":"United States","iso":"US","kind":"country"},{"name":"Oregon","iso":null,"kind":"city"}],"hiring_excludes":[],"relocation_offered":false,"industries":["Clinical Trial Sites & Recruitment"],"lifecycle":[{"event":"open","at":"2026-10-23T21:49:30Z"}],"visa":[],"liveness":{"score":90,"band":"hot","label":"Hiring now","p_open":1,"p_active":0.903,"p_room":1,"age_days":10,"expected_fill_days":51,"reasons":["conf:3","velocity","win:early","comp:junior,attention"],"computed_at":"2026-11-03T05:54:40Z"},"pay":{"stated_usd_annual":72000,"is_top_pay":true},"html_url":"https://alion.io/job/care-access-data-coordinator","json_url":"https://alion.io/job/care-access-data-coordinator.json","meta":{"generated_at":"2026-11-03T07:15:45Z","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":10156,"day_limit":null,"remaining_today":null,"minute_limit":300,"resets_at":"2026-11-04T00:00:00Z"}},"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":19845},"rest":"https://alion.io/mcp/rest/get_company?id=19845"},"human":"https://alion.io/catalog?offer=company.slices&for=job%2Fcare-access-data-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%2Fcare-access-data-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%2Fcare-access-data-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/care-access-data-coordinator\", \"note\": \"what you need it for\"}"},"human":"https://alion.io/catalog?offer=company.verify&for=job%2Fcare-access-data-coordinator"}],"agent":{"mcp":"https://alion.io/mcp/jobs","mcp_open":"https://alion.io/mcp/open","next":[{"tool":"get_job","arguments":{"id":3181919}},{"tool":"search_jobs","arguments":{"company":"careaccess.com","detail":"compact"}},{"tool":"match_people","arguments":{"job_id":3181919},"note":"people open to offers who fit this vacancy"}],"note":"The same data through MCP tools: https://alion.io/mcp/open needs no sign-in (compact searches, postings, people); https://alion.io/mcp with an Alion account has everything. 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