Clinical Research Coordinator

ONO Clinical Research is a growing research site organization based in the Phoenix, Arizona area. We conduct high-quality clinical trials within established medical practices, allowing us to leverage strong patient relationships, experienced investigators, and access to diverse patient populations.Our team brings extensive experience in clinical research and patient care across a range of therapeutic areas. We are committed to maintaining the highest standards of patient safety, regulatory compliance, data quality, and study execution while creating a positive experience for both our patients and research partners.At ONO Clinical Research, we value collaboration, attention to detail, professionalism, and a genuine commitment to advancing medical research. As a growing organization, we offer team members the opportunity to make a meaningful impact while working in a supportive, hands-on research environment.Role DescriptionThe Clinical Research Coordinator (CRC) is a full-time position based in Phoenix, AZ. The CRC is responsible for coordinating and supporting the day-to-day conduct of clinical trials in a practice-based research setting. Responsibilities include coordinating study visits, preparing and maintaining required study documentation, and ensuring compliance with study protocols, Good Clinical Practice (GCP), regulatory requirements, and site procedures.The CRC will obtain and document informed consent, maintain accurate source documentation and study records, complete and support case report form (CRF) and electronic data capture (EDC) activities, and assist with data queries and resolution. Additional responsibilities include scheduling and communicating with study participants, conducting study-related activities and assessments as delegated, collaborating closely with physician investigators and research staff, tracking study timelines and visit requirements, and supporting overall study quality and compliance across assigned trials.The successful candidate will be organized, detail-oriented, patient-focused, and comfortable working in a clinical practice environment. The CRC will play an important role in ensuring a positive participant experience while maintaining the highest standards of research conduct, data quality, and regulatory compliance.QualificationsClinical Research Experience: At least one year of clinical research experience, preferably in a regulated healthcare or clinical trial setting.Education and Clinical Background: Bachelor’s degree, CMA, LPN, RN, or equivalent combination of education and clinical research experience.Informed Consent and Participant Protection: Strong understanding of informed consent procedures, participant rights, confidentiality, and ethical principles related to clinical research.Study Conduct and Compliance: Ability to understand, follow, and appropriately apply study protocols, GCP/ICH guidelines, site procedures, and regulatory requirements.Regulatory Knowledge: Familiarity with IRB processes, essential study documentation, and regulatory requirements applicable to clinical research.Technology Skills: Familiarity with electronic data capture (EDC), clinical trial management systems (CTMS), and standard office software.Organization and Attention to Detail: Strong organizational and time-management skills with the ability to manage multiple studies, competing priorities, and study timelines while maintaining accurate documentation.Communication Skills: Excellent written and verbal communication skills, with the ability to communicate professionally and effectively with study participants, investigators, sponsors/CROs, and multidisciplinary research and clinical teams.Professional Attributes: Ability to work independently and collaboratively in a busy clinic and research environment while maintaining professionalism, confidentiality, and a strong commitment to participant safety and research quality.Preferred Qualifications: Experience in outpatient or practice-based clinical research, experience working with physician investigators, and bilingual communication skills.