{"id":2724997,"url":"https://alion.io/job/centricity-research-research-assistant","title":"Research Assistant","company":{"id":4420651,"name":"Centricity Research","domain":"centricityresearch.com","url":"https://alion.io/company/centricityresearch","size_band":null,"is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Rippling","truth_index":null},"role":"Science & Research","role_family":"Science & Research","seniority":null,"employment_type":"part_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Morehead City, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":68000,"max_usd":185000,"period":"year","method":"role_country_seniority_unknown","sample_n":3587},"experience_years_min":null,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GCP","optional":false},{"name":"Microsoft Office","optional":false}],"status":"live","first_seen_at":"2026-10-16T15:19:14Z","employer_posted_date":"2026-10-16","last_verified_at":"2026-10-24T13:08:34Z","board_verified":true,"closed_at":null,"days_open":8,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":8},"description":"Join the Centricity Research Team!\nCentricity Research is one of the largest clinical research networks in North America. We are a fully centralized Integrated Research Organization (IRO) specializing in conducting Phase I-IV clinical trials in over 35 therapeutic areas: inpatient and outpatient; pharmaceutical, biotechnology, and medical device trials.\nPart Time Research Assistant (RA)\nAbout the Role\nWe’re looking for a part-time Research Assistant (RA) to support the successful execution of clinical research studies from start to finish. This position is scheduled Monday through Friday, 9:00 a.m. to 1:00 p.m., and is fully onsite at our Morehead City, North Carolina site. In this role, you’ll work closely with Investigators, Clinical Research Coordinators (CRCs), and the wider site team to ensure studies run smoothly, safely, and in full compliance with protocol and regulations. This hands-on role is varied - some days you’ll recruit and screen participants, other days you’ll collect data, process samples, or keep study documentation organized and accurate. Your work will directly contribute to advancing clinical research that makes a difference in patients’ lives.\nPlease Note: This role is 100% onsite in Morehead City, North Carolina and requires working Monday through Friday, 9:00 a.m. to 1:00 p.m. Remote and hybrid work arrangements are not available.\nWhat You’ll Do\nStudy Protocol & Safety: Conduct study activities in compliance with GCP, SOPs, and protocols; monitor participant safety; and perform scheduled visits and assessments (e.g., vitals, ECGs). \nRecruitment & Enrollment: Support recruitment efforts, screen participants, obtain informed consent, and maintain accurate documentation. \nStudy Visit Execution: Perform delegated clinical tasks such as phlebotomy, sample collection/shipping, point-of-care testing, and investigational product accountability. \nData Integrity & Compliance: Complete source documents and CRFs, maintain CTMS records, report adverse events promptly, and ensure investigational product inventory and storage compliance. \nSite & Administrative Support: Prepare for monitoring visits and audits, maintain ISF, organize exam rooms and labs, assist with scheduling and participant check-in/out, and support outreach events.\nYou Might Be a Great Fit If You:\nHave a degree in a health, science, or research-related field or equivalent hands-on experience in a healthcare or clinical setting.\nAre comfortable with clinical tools like blood pressure monitors, ECG machines, or point-of-care testing devices (or are eager to learn).\nHave strong attention to detail and can maintain accurate, compliant documentation.\nEnjoy working in a fast-paced environment with changing priorities.\nCommunicate clearly and professionally with participants, colleagues, and external partners.\nAre tech-savvy and comfortable navigating Microsoft Office and clinical data systems.\nThrive in a team environment but can also work independently.\nBring a proactive, problem-solving mindset to every challenge.\nWhy Centricity Research?\nOur Mission\nWe connect people to scientific advancements through groundbreaking research within a deeply human experience.\nOur Core Values\nQuality: We aim for excellence and integrity in everything we do - because lives depend on it.\nCare: We show up for each other, our customers, and our mission - always going the extra mile.\nBe the Change You Seek: We're adaptable, forward-thinking, and constantly improving - for the betterment of all.\nOne Team: We collaborate, support one another, and succeed together.\nGrow for Good: We grow with purpose - to expand access to research and improve global health.\nOwn It: We take initiative, deliver results, and follow through - with passion and accountability.\nBenefits\nComprehensive health, dental, and vision insurance\nEnhanced EAP - mental health support\nFlexible PTO + paid holidays\nContinuing education reimbursement\n401(k) / RRSP with company match and immediate vesting\nReady to Apply?\nWe’d love to hear from you - apply now!\nWe’re an equal opportunity employer committed to building a diverse and inclusive workplace. 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