Local Contract Clinical Research Coordinator

Company: LanceSoft
Location: Fullerton
Posted on: March 31, 2026

Job Description:

Job Description LanceSoft is seeking a local contract Clinical Research Coordinator for a local contract job in Fullerton, California. Job Description & Requirements - Specialty: Clinical Research Coordinator - Discipline: Allied Health Professional - Start Date: 04/27/2026 - Duration: 13 weeks - 40 hours per week - Shift: 8 hours, days - Employment Type: Local Contract Oncology Clinical Research Coordinator Required Qualifications: - Minimum of 2 years of experience in an oncology-focused clinical research setting involving direct patient management (5 years preferred). - Hands-on experience with patient-facing responsibilities, including: - Informed consent - Vital signs and EKG collection - Lab processing - Medication dispensing - Documentation and data entry - Strong knowledge of clinical research processes and regulatory requirements. - Mandatory experience with EPIC (Electronic Medical Records system). - Proficiency in Microsoft Office Suite (Outlook, Word, Excel) and MS Teams. Additional Requirements: - Experience in device trials or data-only trials will not be considered. - Strong organizational, communication, and multitasking skills. - Ability to work independently while managing multiple studies. - Commute within 30 minutes is preferred due to local traffic considerations. Preferred Qualifications: - Bilingual skills (Spanish or Korean) are a plus. Job Summary:/nThe Oncology Clinical Research Coordinator is responsible for managing the day-to-day operations of multiple clinical research studies under the supervision of the Medical Office Administrator. This role involves close collaboration with the Principal Investigator (PI), patients, sponsors, and the Institutional Review Board (IRB) to ensure all study activities are conducted in compliance with protocols, regulatory requirements, and Good Clinical Practice (GCP/ICH) guidelines. The coordinator ensures accurate and timely documentation while maintaining high standards of patient care and study integrity./n/nKey Responsibilities:/n/nManage daily operations of assigned clinical research studies./nReview and understand all study-related communications and ensure proper documentation of written and verbal correspondence./nAct as a liaison between sponsors, monitors, patients, physicians, laboratories, and other stakeholders./nEnsure accurate and timely data entry into electronic data capture (EDC) systems within 7 days of patient visits./nOversee investigational product (IP) accountability, including documentation, storage conditions, temperature logs, expiration tracking, and return or destruction processes./nCoordinate patient participation, ensuring compliance with study protocols, visit schedules, and at-home requirements./nRecruit, screen, and retain study participants./nProcess, package, and ship biological samples according to protocol and laboratory requirements./nMaintain organized and complete study documentation, including regulatory binders and participant files./nPerform regulatory activities and ensure compliance with GCP/ICH and study protocols./nCoordinate study-related appointments, lab work, and follow-ups with patients./nParticipate in investigator meetings and support study start-up and close-out activities./nIdentify and support opportunities for new clinical research studies./nMaintain inventory and control of study medications and supplies. About LanceSoft Established in 2000, LanceSoft is a Certified MBE and Woman-Owned organization. Lancesoft Inc. is one of the highest rated companies in the industry. We have been recognized as one of the Largest Staffing firms and ranked in the top 50 fastest Growing Healthcare Staffing firms in 2022. Lancesoft offers short- and long-term contracts, permanent placements, and travel opportunities to credentialed and experienced professionals throughout the United States. We pride ourselves on having industry leading benefits. We understand the importance of partnering with an expert who values your needs, which is why we’re 100% committed to finding you an assignment that best matches your career and lifestyle goals. Our team of experienced career specialists takes the time to understand your needs and match you with the right job Lancesoft has been chosen by Staffing Industry Analysts as one of the Best Staffing Firms to Work for.LanceSoft specializes in providing Registered Nurses, Nurse Practitioners, LPNs/LVNs, Social Workers, Medical Assistants, and Certified Nursing Assistants to work in Acute Care Centers, Skilled Nursing Facilities, Long-Term Care centers, Rehab Facilities, Behavioral Health Centers, Drug & Alcohol Facilities, Home Health & Community Health, Urgent Care Clinics, and many other provider-based facilities. Benefits - Weekly pay - Medical benefits

Keywords: LanceSoft, Carson , Local Contract Clinical Research Coordinator, Healthcare , Fullerton, California