Lead Clinical Research Coordinator

Job Overview As a Lead Research Clinical Coordinator, you will play a crucial role in conducting research activities within a clinical setting. You will be responsible for overseeing and participating in various research projects to advance medical knowledge and improve options available within our clinic for patient care. You will responsible for all aspects of study startups, site initiation, budgeting, IRB submissions, and most importantly, regulatory and compliance oversight. Duties Work with sponsor for budgeting and finalizing site contracts Complete site initiation and start-up Supervise and coordinate clinical development activities Ensure compliance with Good Clinical Practice (GCP) guidelines and HIPAA regulations Submit FDA and IRB documents during study duration Create appropriate source documents Be familar and able to upload data to EDC Effectively communicate study issues with the spondor , CRO and IRB as needed Utilize medical terminology effectively in research documentation -- Conduct blood sampling and vital sign measurements Skills Proficiency in data management and analysis Strong understanding of clinical research methodologies Knowledge of medical terminology and clinical trial processes Experience in supervising research activities Familiarity with clinical laboratory procedures Ability to adhere to HIPAA regulations in handling patient data Job Type: Full-time Pay: $50,000.00 - $109,235.00 per year Benefits 401(k) Dental insurance Health insurance Paid time off Vision insurance Medical Specialty Cardiology Gastroenterology Oncology Schedule 8 hour shift Ability to Relocate Indianapolis, IN 46290: Relocate before starting work (Required) Work Location: In person #J-18808-Ljbffr The Voluntary Protection Programs Participants' Association, Inc