{"id":1151940,"url":"https://alion.io/job/iqvia-clinical-research-associate-2-iqvia-2","title":"Clinical Research Associate 2, IQVIA","company":{"id":4918,"name":"IQVIA","domain":"iqvia.com","url":"https://alion.io/company/iqvia","size_band":"5000+","is_staffing_agency":false,"is_intermediary":false,"ats_vendor":"Workday","truth_index":{"grade":"B","score":83,"open_postings":441,"ghost_share":0.002,"stale_share":0.878,"repost_share":0.011,"time_to_fill_p50_days":16,"computed_at":"2026-09-23T05:45:00Z"}},"role":"Science & Research","role_family":"Science & Research","seniority":"junior","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"hiring_geo_confidence":"structured","locations":["Durham, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":{"min":74500,"max":197500,"currency":"USD","period":"year","gross":null,"usd_annual":197500},"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}],"status":"live","first_seen_at":"2026-09-23T18:11:58Z","employer_posted_date":"2026-09-23","last_verified_at":"2026-09-23T18:11:46Z","board_verified":true,"closed_at":null,"days_open":0,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":0},"description":"IQVIA is seeking a Clinical Research Associate II with independent on-site monitoring experience to join our team. We are looking for professionals with experience in one or more of the following therapeutic areas:\nCentral Nervous System (CNS)\nCardiovascular\nObesity\nMASH/NASH\nJob Overview\nConduct site selection, initiation, routine monitoring, and closeout visits in accordance with GCP, ICH, and applicable regulatory requirements.\nBuild strong relationships with investigative sites and provide protocol, process, and study-specific training.\nMonitor study progress, including site activation, patient recruitment, enrollment, data collection, and query resolution.\nEvaluate site performance and compliance, identifying risks and escalating quality concerns when appropriate.\nEnsure study documentation, regulatory records, and Trial Master File (TMF) requirements are maintained accurately and are inspection-ready.\nPrepare monitoring reports, follow-up communications, and other required study documentation.\nCollaborate with cross-functional study teams to support successful project delivery and achieve study milestones.\nSupport patient recruitment and retention initiatives at the site level.\nAssist with site financial and administrative activities, including invoice management, when applicable.\nQualifications\nBachelor's degree required \nMinimum 1 year of independent on-site monitoring experience in a CRO, biotech or pharmaceutical\nWorking knowledge of GCP, ICH, and clinical trial regulations.\nStrong communication, organizational, and problem-solving skills.\nProficiency with Microsoft Office applications.\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 $74,500.00 - $197,500.00. 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":3316,"description_truncated":false,"requirements":{"experience_years_min":1,"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 Research","Biotechnology","Health Care"],"lifecycle":[{"event":"open","at":"2026-09-23T18:11:58Z"}],"liveness":{"score":86,"band":"hot","label":"Hiring now","p_open":1,"p_active":0.86,"p_room":1,"age_days":0,"expected_fill_days":16,"reasons":["conf:4","win:early","comp:junior,brand"],"computed_at":"2026-09-23T22:16:45Z"},"pay":{"stated_usd_annual":197500,"is_top_pay":true},"html_url":"https://alion.io/job/iqvia-clinical-research-associate-2-iqvia-2","json_url":"https://alion.io/job/iqvia-clinical-research-associate-2-iqvia-2.json","meta":{"generated_at":"2026-09-23T22:16:45Z","cache_seconds":300,"methodology":"https://alion.io/methodology","terms":"https://alion.io/terms","contact":"https://alion.io/contact","api":"https://alion.io/developers"}}