Clinical Research Coordinator

Clinical Research Coordinator The Plastics Clinic, LLC Draper, UT Job Details 4 hours ago Benefits Paid holidays Health insurance Dental insurance Paid time off Vision insurance Retirement plan Qualifications CCRC Informed consent Inventory management Adverse event reporting Clinical incident reports BLS Certification Filing Mid-level Clinical research protocol review Research project coordination Data integrity and documentation Bachelor's degree Clinical data entry Data quality monitoring Informed consent procedures implementation Research compliance clinical trial records management Organizational skills Clinical trial patient safety management Implementing research protocols Patient recruitment Communication with regulatory authorities for clinical trials Patient interaction Patient counseling Clinical quality assurance standards Patient education Ethical review application preparation Communication skills FDA regulations Research compliance audit records management Time management Full Job Description Position Overview We're looking for a highly organized and detail-oriented Clinical Research Coordinator to join our team and oversee the day-to-day coordination and management of clinical research studies in compliance with federal regulations, institutional policies, and Good Clinical Practice (GCP) guidelines. This role serves as the hands-on liaison between study sponsors, investigators, regulatory bodies, and research participants, ensuring the integrity and ethical conduct of all assigned protocols. Working under the Director of Clinical Research, the CRC plays a critical role in advancing research goals while safeguarding participant safety and data quality. Responsibilities Study Initiation and Management Reviews protocols and assesses study feasibility Sets up and organizes study files, including regulatory documentation Prepares documents for Institutional Review Board (IRB) submission Maintains adequate inventory of study supplies Participant Recruitment and Care Screens, recruits, and enrolls participants based on inclusion/exclusion criteria Conducts the informed consent process and ensures comprehension Coordinates study visits and ensure procedures are done per protocol Acts a liaison between participants, investigators, and sponsors Data Management & Compliance Ensures adherence to GCP, FDA, and IRB guidelines Collects and enters data into Case Reports Forms (CRFs) Reports adverse events and protocol violations to the PI and IRB Handles data queries and prepares for monitoring visits Any other responsibilities as needed by the supervisor. Qualifications Bachelor's degree in life science, health-related field, or equivalent experience Minimum of 2 years of clinical research experience, strongly preferred Additional certifications such as GCP, CCRC, or BLS, preferred Strong attention to detail and organizational skills Excellent time management skills and ability to manage multiple protocols simultaneously Ability to work independently and collaboratively with multidisciplinary teams Excellent communication and patient education skills Why The Plastics Clinic & Spa? We're a growing, physician-led aesthetic practice with a reputation for excellence, a tight-knit team culture, and a genuine commitment to our guests and our people. We invest in training, growth, and building careers — not just filling seats. This is a foundational role that will set the tone for our amazing new locations! Here are a few things we offer: Competitive compensation & bonus eligibility Comprehensive benefits package with medical, dental, vision, and retirement plan with company match Top-of-the-line spa perks and access to discounts Industry-leading Paid Time Off & paid holidays Opportunities for growth and development alongside a world-class management and clinical team E04JI802s7ag4097pm3