Clinical Research Coordinator

CLINICAL RESEARCH COORDINATOR

Responsibilities Study Coordination Work closely with principal investigators to plan and execute clinical research studies. Ensure compliance with study protocols, regulatory guidelines, and ethical standards. Coordinate study activities, including participant recruitment, enrollment, and retention. Schedule participant visits and coordinate study procedures. Participant Management Screen and recruit eligible participants according to study criteria. Obtain informed consent from participants and ensure understanding of study procedures. Provide support and guidance to participants throughout the study duration. Coordinate participant follow-up visits and assessments. Data Management Collect, record, and maintain accurate and complete study data. Enter data into study databases or electronic data capture systems. Ensure data quality and integrity through regular monitoring and verification. Regulatory Compliance Assist with preparation and submission of regulatory documents, such as Institutional Review Board (IRB) applications and informed consent forms. Maintain study documentation and regulatory files in accordance with regulatory requirements. Monitor and ensure compliance with Good Clinical Practice (GCP) guidelines and applicable regulations. Communication and Collaboration Serve as a liaison between study sponsors, investigators, research staff, and participants. Coordinate communication and meetings with study team members and stakeholders. Collaborate with interdisciplinary teams to resolve study-related issues and challenges. Administrative Tasks Assist with budgeting, financial tracking, and procurement related to study activities. Prepare and maintain study-related documentation, including study manuals, SOPs, and training materials. Coordinate study logistics, such as equipment and supplies procurement. Qualifications Previous experience in oncology clinical research coordination Is a bonus. Knowledge of clinical research regulations, GCP guidelines, and ethical principles. Strong organizational skills and attention to detail. Excellent communication and interpersonal skills. Proficiency in computer applications, including MS Office and electronic data capture systems. Ability to work independently and as part of a team in a fast-paced environment. Certification in clinical research (e.g., ACRP, SOCRA) desirable but not required. Additional Requirements Willingness to adhere to strict confidentiality requirements. Flexibility to work occasional evenings or weekends, depending on study requirements. Ability to travel to off-site locations for participant visits or study-related meetings, if necessary. #J-18808-Ljbffr Community Clinical Trials