Research Study Coordinator

Job Overview
We are seeking a highly motivated and detail-oriented Research Study Coordinator to join our dynamic clinical research team. In this pivotal role, you will oversee the coordination and management of clinical studies, ensuring adherence to regulatory standards and research protocols. Your energetic approach will drive the successful execution of research projects, from participant recruitment to data collection and compliance management. This position offers an exciting opportunity to contribute to cutting-edge healthcare research, supporting advancements that improve patient outcomes worldwide.

Duties

• Coordinate all aspects of clinical trials, including participant screening, enrollment, and follow-up procedures
• Monitor patient progress by recording vital signs, blood sampling, and other clinical assessments in accordance with study protocols
• Review and ensure accuracy of study documentation, including consent forms, case report forms, and regulatory submissions
• Manage data collection processes using statistical software and adhere to CDISC standards for data formatting and reporting
• Supervise research staff and collaborate with multidisciplinary teams to maintain high standards of clinical quality assurance and compliance with FDA regulations and ICH GCP guidelines
• Conduct clinical laboratory procedures such as phlebotomy and blood sampling while maintaining safety standards
• Oversee project timelines, budgets, and documentation review to ensure seamless progress of research initiatives

Requirements

• Proven supervising experience in a clinical or research setting with strong leadership skills
• Knowledge of medical terminology, clinical development processes, and healthcare compliance standards including HIPAA and FDA regulations
• Familiarity with clinical research methods, ethical guidelines, and Good Clinical Practice (GCP) certification from a recognized issuer such as ICH GCP certificate
• Experience with data management systems, statistical software, and Microsoft Office suite for documentation and reporting purposes
• Hands-on experience in clinical laboratory procedures like blood sampling and vital signs measurement
• Strong understanding of clinical trials management, research project management, and compliance management practices
• Excellent analysis skills combined with attention to detail for reviewing documentation and ensuring protocol adherence
• Ability to navigate complex regulatory environments while maintaining high standards of clinical ethical guidelines

Join us in advancing healthcare through innovative research! This paid position offers an engaging environment where your expertise will directly impact the development of new therapies. We value energetic professionals committed to excellence in clinical research practices who thrive in collaborative settings. If you’re ready to make a difference in patient care while developing your career in a fast-paced research environment, we want to hear from you!

Pay: $18.00 per hour

Expected hours: 4.0 – 12.0 per week

Work Location: In person