{"id":4144496,"url":"https://alion.io/job/iqvia-research-coordinator-3","title":"Research Coordinator","company":{"id":4918,"name":"IQVIA","domain":"iqvia.com","url":"https://alion.io/company/iqvia","size_band":"5000+","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"B","score":78,"open_postings":554,"ghost_share":0.018,"stale_share":0.794,"repost_share":0.042,"time_to_fill_p50_days":24,"computed_at":"2026-11-11T05:49:22Z"}},"role":"Administrative","role_family":"Administrative","seniority":"senior","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Irving, United States","Houston, United States","United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":{"min":43400,"max":108200,"currency":"USD","period":"year","gross":null,"usd_annual":108200},"salary_estimate":null,"experience_years_min":5,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"CAPA","optional":false}],"status":"live","first_seen_at":"2026-11-11T00:00:00Z","employer_posted_date":"2026-11-11","last_verified_at":"2026-11-12T06:33:29Z","board_verified":true,"closed_at":null,"days_open":1,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":1},"description":"The Research Coordinator advocates for patient safety and protocol integrity, adheres to patient care standards, and communicates effectively to ensure effective conduct of clinical trials and quality patient care. Research Coordinators assist with screening patients, schedule, and oversee all on-study requirements. Research Coordinators attend study teleconferences with sponsors and clinical research organizations to assure continuity of information.\nEssential Duties and Responsibilities\nEssential and other important responsibilities and duties may include but are not limited to the following:\nProtocol Compliance\nIdentifies primary and secondary study objectives and outcome measures\n\nAdheres to applicable federal, state, and institutional regulations, policies, and procedures related to clinical research\n\nComplies with NEXT Oncology SOPs\n\nParticipates in providing timely, informative, and accurate communication with the interdisciplinary team to ensure protocol compliance and timelines of protocol-related procedures\n\nCollaborates with the Principal Investigator, pharmacy, and other appropriate personnel to ensure proper use of and accountability for study drugs\n\nProvides protocol specific education to clinical staff\n\nFacilitates and participates in the preparation for an conduct of meetings/teleconferences with sponsors, monitors, and auditors\n\nProvides timely, accurate, and complete reporting of serious adverse events, unanticipated problems, deviations, violations, and noncompliance to the IRB and sponsor\n\nContributes to the development of corrective and preventive action plans for unanticipated problems, deviations, violations, and issues of noncompliance\n\n Informed Consent\nIdentifies and intervenes to address barriers to effective informed consent discussions and decision making (e.g., literacy, capacity, language, distress, lack of time, therapeutic misconception)\n\nDescribes and abides by institutional policy and processes for informed consent\n\nEnsures that the most current version of the IRB approved protocol consent document is used by the physician investigator when consenting or re-consenting a patient\n\nCollaborates with the physician investigator to ensure initial and ongoing consent process is performed and documented\n\nAssesses ongoing consent through discussions with patients and reinforcement of education\n\nAssesses patient’s understanding of the information provided during the informed consent process\n\nEnsures timely re-consenting as needed by the physician investigator\n\nDemonstrates understanding of tiered consent process when optional correlative studies (e.g., biospecimen, quality of life, patient-reported outcomes collections) are involved\n\nConfirms informed consent is obtained prior to performing any study specific tasks\n\n Management of Clinical Trial Patients\nCollaborates with the investigator to ascertain study patient eligibility for a clinical trial, including documentation of criteria specified in the protocol\n\nEducates the patient and family regarding protocol participation\n\nProvides patient education regarding required study procedures\n\nIf the Research Coordinator is a Registered Nurse, educates the patient and family regarding clinical condition, and/or disease process. If the Research Coordinator is not a RN, he/she will schedule educational time with a RN\n\nIf the Research Coordinator is a Registered Nurse, identifies patients who require increased nursing assessment and management in addition to the clinical trial requirements and collaborate with other members of the healthcare team to ensure patient safety. If the Research Coordinator is not an RN, he/she will schedule educational time with a RN\n\nCoordinates, schedules, and ensures timely completion of protocol-required events and other requirements (e.g., pharmacokinetics or -dynamics, scans, study visits, QOL,)\n\nAssesses individual patients for physical, psychosocial, and financial factors that could impact adherence with study requirements and implement interventions as necessary\n\nEvaluates patient’s adherence to and documentation of self-administered protocol agents and the return of such agents\n\nCollaborates with the investigator to determine disease response as defined by the protocol and communicates findings to the study team and other care providers\n\nEvaluates patient’s adherence to and documentation of self-administered protocol agents and return of such agents\n\nCollaborates with the investigator to determine if any treatment schedule or drug dose modification is necessary and communicates findings to the study team and other care providers\n\nEnsures appropriate communication between research and clinical staff related to patient-specific care needs\n\nEnsures evidence-based symptom management as permitted by the protocol\n\nDocumentation and Document Management\nDocuments all patient encounters in the legal medical record per licensure and institutional requirements\n\nObtains documents from outside providers or laboratories that are needed as part of the research data\n\nEducates other research team members and clinical staff regarding appropriate and accurate source documentation for patients of in clinical trials\n\nAssesses documentation or discrepancies and ensures that inaccurate or discrepant documentation is addressed in the medical record or other source documents\n\nMaintains the privacy and confidentiality of patients' source documents\n\nMaintains specified study documents in the Research Coordinator files\n\nParticipates in the development of approved source documents, templates, or forms\n\nData Management and Information Technology\nAdheres to the data management plan per NEXT SOPs and sponsor data management plan\n\nAssists in troubleshooting data entry issues\n\nEnsures that relevant data from source documents are abstracted and entered into CRFs in a timely and accurate manner\n\nEnsure that data recorded on the CRFs can be verified within the source documents\n\nParticipates in quality control activities to ensure data integrity, including timely responses to database or sponsor queries\n\nEnters data into electronic data capture for SAEs as appropriate\n\nRequired Education and Experience \nThe Research Coordinator must be knowledgeable of standard research and oncology care practices\n\nTypically requires 5 or more years of experience\n\nCurrent Texas or Virginia Registered Nursing License for RNs\n\nBachelor's degree required for non-RNs\n\nOncology clinical trial experience preferred\n\nResearch Coordination experience preferred\n\nWhy Join Us?\nAt NEXT Oncology (an Avacare Business), you’ll be part of a mission-driven team that values collaboration, precision, and patient safety. Our team is known for its supportive culture, strong communication, and commitment to excellence in clinical research.\nIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com\nIQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe\nIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.\nThe potential base pay range for this role, when annualized, is $43,400.00 - $108,200.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.","description_format":"text","description_chars":8486,"description_truncated":false,"requirements":{"experience_years_min":5,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":{"level":"bachelor","optional":false},"security_clearance":false,"languages":[]},"benefits":[],"hiring_locations":[],"hiring_excludes":[],"relocation_offered":false,"industries":["Clinical Trial Services (CRO)","Health Data & Interoperability","Clinical Trial Software","Healthcare & Life Sciences Consulting"],"lifecycle":[{"event":"open","at":"2026-11-12T06:33:29Z"}],"visa":[{"country":"US","licensed_sponsor":true,"adverts_offering_sponsorship_24m":0,"sanctioned_now":false,"evidence":"H-1B filings in 12 months: 142 · green card filings: 13","filings_12m":142,"filings_prev_12m":166,"green_card_filings_12m":13,"median_offered_wage_usd":141339,"route":null,"cap_exempt":false,"checked_at":"2026-11-12T07:36:15+00:00","sources":["US Department of Labor: LCA disclosure data (H-1B, H-1B1, E-3)","US Department of Labor: PERM disclosure data (green cards)"],"filings_for_role_12m":0}],"liveness":{"score":86,"band":"hot","label":"Hiring now","p_open":1,"p_active":0.86,"p_room":1,"age_days":1,"expected_fill_days":24,"reasons":["conf:2","win:early","comp:brand"],"computed_at":"2026-11-12T08:52:04Z"},"pay":{"stated_usd_annual":108200,"is_top_pay":true},"html_url":"https://alion.io/job/iqvia-research-coordinator-3","json_url":"https://alion.io/job/iqvia-research-coordinator-3.json","meta":{"generated_at":"2026-11-12T08:52:04Z","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":17859,"day_limit":null,"remaining_today":null,"minute_limit":300,"resets_at":"2026-11-13T00:00:00Z"}},"offers":[{"id":"company.slices","title":"One company in depth, by slice","status":"live","price":{"credits":0.1,"usd":0.01,"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":4918},"rest":"https://alion.io/mcp/rest/get_company?id=4918"},"human":"https://alion.io/catalog?offer=company.slices&for=job%2Fiqvia-research-coordinator-3"},{"id":"market.stats","title":"A market slice: pay, demand and time to fill","status":"live","price":{"credits":2,"usd":0.2},"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%2Fiqvia-research-coordinator-3"},{"id":"job.search","title":"Open jobs by role, technology, place, pay and visa","status":"live","price":{"credits":0.1,"usd":0.01},"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%2Fiqvia-research-coordinator-3"},{"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/iqvia-research-coordinator-3\", \"note\": \"what you need it for\"}"},"human":"https://alion.io/catalog?offer=company.verify&for=job%2Fiqvia-research-coordinator-3"}],"agent":{"mcp":"https://alion.io/mcp/jobs","mcp_open":"https://alion.io/mcp/open","next":[{"tool":"get_job","arguments":{"id":4144496}},{"tool":"search_jobs","arguments":{"company":"iqvia.com","detail":"compact"}},{"tool":"match_people","arguments":{"job_id":4144496},"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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