Job Title

Drive impactful clinical studies with Providence Research as a Clinical Research Coordinator. This role involves supporting diverse investigator teams while ensuring compliance and high data quality. As a vital part of Providence Research, you will coordinate multiple clinical research studies under the supervision of various Principal Investigators. Your responsibilities include facilitating workflows, managing ethical approvals, and ensuring adherence to regulatory standards. Adaptability and initiative are crucial in this collaborative and agile position, requiring effective communication and multitasking across different study environments. Key Responsibilities: Coordinate and support multiple clinical research studies Act as liaison for research teams and hospital departments Facilitate study start-up, conduct, and close-out activities Ensure compliance with ethical standards and regulations Maintain data quality across all research activities Requirements: Bachelor''s degree in health or social sciences Minimum four years of clinical research experience Certification from SOCRA, ACRP, or similar preferred Strong interpersonal and communication skills Proficiency in electronic data capture systems Bring your expertise and passion for clinical research to enhance patient care at Providence Research. #J-18808-Ljbffr