Clinical Research Assistant

RESEARCH ASSISTANT – CLINICAL RESEARCH (ONCOLOGY)HIGHLIGHTSJoin a rapidly growing clinical research organization with 30+ locations across 10+ states and continued expansion planned throughout 2026 and beyondWork directly with patients and an experienced research team supporting oncology clinical trials$26.00- $32.00/hour, depending on clinical research experience and skill setStrong opportunity for career development within a fast-growing, entrepreneurial clinical research networkComprehensive benefits including health, dental, and vision insurance; 15 days of PTO; 10 company holidays; and a 401(k) with a 4% employer matchAdditional benefits include tuition reimbursement, parental leave, life and disability insurance, employee assistance programs, and moreCOMPANYOur client is a fast-growing clinical research organization with more than 30 locations across 10+ states and a broad portfolio of clinical trials across multiple therapeutic areas. This opportunity sits within an established oncology research operation in Century City. With continued expansion planned throughout 2026 and beyond, the organization offers an entrepreneurial environment with significant opportunities for employees to grow their careers.POSITIONWe are seeking a Research Assistant with prior clinical research experience to join our client's Century City team. This is a full-time, on-site position supporting Clinical Research Coordinators and other site staff with patient visits, study documentation, recruitment, and day-to-day trial activities. The ideal candidate enjoys patient interaction, is comfortable working in a busy research environment, and brings strong attention to detail.RESPONSIBILITIESAssist with clinical trial visits and protocol-required procedures, including vital signs, EKG/ECGs, phlebotomy, injections, and other clinical tasks based on experienceSupport informed consent, patient scheduling, recruitment, and enrollment activitiesMaintain accurate source documentation, study data, and case report formsAssist with lab samples, study supplies, kits, and other materials needed for ongoing trialsCommunicate study updates, patient information, and potential adverse events to the appropriate research team membersWork closely with CRCs, investigators, sponsors, and other site personnel while following GCP and study requirementsQUALIFICATIONSAt least 2 years of clinical research experience required; oncology research experience is strongly preferredBachelor's degree preferred, but not requiredHands-on clinical skills such as phlebotomy, EKG/ECG, vital signs, and injections are preferredWorking knowledge of GCP, FDA/ICH requirements, medical terminology, and clinical research documentationExperience with electronic source documentation or similar clinical research technology preferredStrong organization, communication, critical thinking, and attention to detail, with the ability to work effectively in a patient-facing research environment