Clinical Trials/Patient Coordinator

Job Summary The post holder will be held accountable to the Regional Manager for the highest standards of operational delivery of the Clinical Trials for which the post holder is appointed to co-ordinate. This includes responsibility for delivering these trials according to clinical trials Good Clinical Practice (GCP), ensuring appropriate resources, including professional skill mix, training and competency are in place at all times. Additionally, this person will ensure practice at the center is safe, performance at CRA visits, external monitoring visits and FDA inspections are planned and executed for optimal success. What you’ll do To ensure that the highest levels of customer/patient care and clinical delivery are maintained at all times To support the development of the business by working closely with clinicians and consultants to maximize business opportunities and recruit patients Adhere to the organization’s policies and SOPs and ensure all members of the clinical trials team are trained and compliant To ensure that all administration is performed accurately and in a timely way including the entry of patient records on all necessary databases and forms To ensure that all patient records are accurate, stored appropriately and all confidential information is retained in accordance with data protection requirements To ensure that the Centre is maintained and presented to the highest standards as expected by the organization and that all equipment is calibrated and maintained in line with best practice To ensure adequate stock within the Center ensuring that it is ordered in a timely way and that stock is controlled To seek feedback from patients as to their experience and record these findings and analyze them to support the ongoing development of the service To be responsible for answering all queries and SAE and related IRB/FDA reporting within the time frames dictated for each study and GCP Private Practice Support Coordinate all patient visits for monoclonal antibody infusions. Schedule appointments, scans, lab tests, and follow-up visits in collaboration with physicians and external providers. Manage appointment confirmations, rescheduling, and patient reminders. Liaise with radiology centers, laboratories, and external medical providers. Work closely with the PC Manager and physicians to ensure an efficient patient flow. Maintain accurate and up-to-date patient medical records. Facilitate secure transmission of medical documents between referring physicians and internal teams. Ensure HIPAA and GDPR compliance in handling patient data. Serve as a point of contact for referring physicians regarding patient progress and documentation. Participate in weekly team meetings to discuss patient updates and workflow improvements. Ensure smooth collaboration between clinical research and PC teams. Perform vital signs assessments (blood pressure, pulse, respiratory rate, temperature, etc.). Conduct electrocardiograms (EKGs) and ensure accurate documentation. Monitor patients during infusion sessions, reporting any concerns to medical staff. Qualifications 3-5 years experience in Clinical Trials Coordination, operation, set-up and delivery. 1-2 years experience in Healthcare setting, preferred. Proficiency in the use of Microsoft Office packages (Word, Excel, PowerPoint) Experience with electronic data capture (EDC) systems (Azalea Health EMR preferred) Re:Cognition Health is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, disability status, protected veteran status, or any other characteristic protected by law. Compensation The pay range for this role is: 65,000 - 70,000 USD per year (Chicago HQ) #J-18808-Ljbffr Re-Cognition-Health-Limited-