Clinical Research Coordinator

Assist in the coordination and execution of clinical research protocols under the supervision of the PI and senior research staff Assist with informed consent and enrollment of study participants in accordance with protocol requirements and ethical guidelines Communicate with study participants to provide education, answer questions, and support adherence to study requirements Monitor study progress and report adverse events, protocol deviations, and other study- related issues to the research team Adhere to site standard operating procedures (SOPs) and Good Clinical Practice (GCP) guidelines Scan, upload, file, and maintain organized study records and documentation Apply critical thinking skills to support efficient study operations and problem resolution Perform other duties as assigned Required Skills: Strong organizational, time management, and attention-to-detail skills with the ability to manage multiple priorities Ability to communicate clearly and professionally with diverse populations Ability to work collaboratively in a fast-paced, team-oriented environment Preferred Skills: Medical Assistant (MA) or Phlebotomy certification preferred, not required. Current CPR/BLS certification preferred, not required. Certification as a Clinical Research Coordinator (e.g., CCRC) or a willingness to obtain certification preferred, not required. An associate’s degree or higher in a health-related field preferred, not required. #J-18808-Ljbffr