Clinical Research Coordinator II

Job Description Posted Tuesday, June 16, 2026 at 5:00 AM Clinical Research Coordinator II Florida Kidney Physicians (FKP) | Jacksonville Beach, FL Powered by Panoramic Science, the Research Division of Panoramic Health Panoramic Health's Clinical Research Division is growing, and we're looking for an experienced Clinical Research Coordinator II to join our Jacksonville Beach team. This is an exciting opportunity to play a leading role in clinical trials that directly impact patients living with chronic kidney disease and related conditions. As part of one of the nation's largest nephrology-focused research networks, you'll work alongside physicians, patients, sponsors, and research professionals to bring innovative therapies to those who need them most. If you're passionate about patient care, clinical research excellence, and making a meaningful difference through medical innovation, we'd love to hear from you. Why Join Us? Be part of a rapidly expanding national clinical research network Contribute to studies that improve outcomes for patients with kidney disease Partner closely with experienced investigators and research leaders Enjoy a stable Monday–Friday schedule with no nights or weekends Opportunity for professional growth, increased responsibility, and career advancement What You'll Do As the Clinical Research Coordinator II, you will lead day-to-day clinical trial operations at the site level while ensuring compliance with protocol requirements, regulatory standards, and Good Clinical Practice (GCP). Review and understand research protocols and study requirements Identify, pre-screen, recruit, and enroll eligible research participants Obtain and document informed consent in accordance with GCP and site SOPs Collaborate with providers, clinic staff, and central research teams to drive enrollment goals Develop and implement workflows that optimize recruitment and study execution Study Management & Compliance Coordinate and schedule participant visits according to protocol requirements Maintain accurate and timely study documentation and source records Complete case report forms (CRFs) and electronic data entry with a high degree of accuracy Ensure adherence to ALCOA documentation principles Manage investigational product accountability and study supplies Collect and process laboratory specimens according to protocol requirements Monitoring & Regulatory Support Prepare for sponsor and CRO monitoring visits Resolve data queries and action items promptly Maintain study logs, temperature records, and accountability documentation Report adverse events and serious adverse events according to sponsor, IRB, and regulatory requirements Support ongoing protocol compliance and quality initiatives What We're Looking For Required Qualifications 3–5 years of clinical research experience as a Clinical Research Coordinator or similar role Strong knowledge of GCP, FDA regulations, and clinical research processes Experience recruiting, consenting, and managing research participants Knowledge of medical terminology and clinical documentation Ability to manage multiple studies simultaneously in a fast-paced environment Excellent organizational, communication, and problem-solving skills Ability to perform basic clinical procedures, including: Vital signs; Height and weight measurements; ECGs Preferred Qualifications Medical Assistant Certification Bachelor's degree in a health-related field ACRP or SOCRA Certification GCP and/or IATA Certification Experience in nephrology, chronic kidney disease (CKD), vascular access, or related therapeutic areas Who Will Thrive in This Role? Self-motivated and proactive Detail-oriented and highly organized Passionate about patient safety and research quality Comfortable building relationships with patients and providers Able to balance multiple priorities while maintaining accuracy and compliance Driven to exceed enrollment and study performance goals Join Our Mission At Florida Kidney Physicians and Panoramic Science, we're transforming the future of kidney care through groundbreaking clinical research. Every study we conduct has the potential to improve lives, advance treatment options, and shape the future of nephrology. If you're ready to take the next step in your clinical research career while making a meaningful impact on patient care, apply today! The Company is committed to the principles of equal employment. We are committed to complying with all federal, state, and local laws providing equal employment opportunities, and all other employment laws and regulations. It is our intent to maintain a work environment which is free of harassment, discrimination, or retaliation because of age, race, color, national origin, ancestry, religion, sex, pregnancy (including childbirth, lactation and related medical conditions), physical or mental disability, genetic information (including testing and characteristics), veteran status, uniformed servicemember status, or any other status protected by federal, state, or local laws. The company is dedicated to the fulfillment of this policy in regard to all aspects of employment, including but not limited to recruiting, hiring, placement, transfer, training, promotion, rates of pay, and other compensation, termination, and all other terms, conditions, and privileges of employment. For information about our Privacy Policy, please visit here #J-18808-Ljbffr