Job Overview We are seeking a dedicated and detail-oriented Clinical Research Coordinator to join our dynamic research team. In this vital role, you will oversee the planning, execution, and management of clinical trials, ensuring compliance with regulatory standards and ethical guidelines. Your expertise will help advance medical research by coordinating study activities, monitoring patient progress, and maintaining meticulous documentation. This position offers an exciting opportunity to contribute to innovative healthcare solutions while working in a collaborative and fast-paced environment. The ideal candidate is passionate about research, possesses strong organizational skills, and has a solid understanding of clinical trial processes. Responsibilities Coordinate all aspects of clinical trials, including participant recruitment, scheduling, and follow-up assessments Monitor patient safety and well-being throughout the study, ensuring adherence to protocols and ethical guidelines Review and verify clinical documentation for accuracy, completeness, and compliance with FDA regulations and ICH GCP standards Manage data collection, entry, and management using electronic medical record (EMR) systems and other data management tools Conduct patient assessments such as vital signs, blood sampling (phlebotomy), and other clinical procedures with precision Supervise research staff and volunteers, providing guidance on study protocols and compliance management Ensure all study activities are documented thoroughly in accordance with CDISC standards and healthcare compliance requirements Qualifications Proven supervising experience in a clinical or research setting with strong project management skills in healthcare environments with at least 2 years of experience Comprehensive knowledge of clinical trials management, including regulatory requirements such as FDA regulations, HIPAA, and clinical ethical guidelines Proficiency in medical terminology, data management software, statistical analysis tools, and EMR systems Certification in ICH Good Clinical Practice (GCP) from a recognized issuer for CA or equivalent is required Experience with clinical laboratory procedures including blood sampling (phlebotomy), analysis skills, and vital signs measurement Familiarity with CDISC standards for data collection and reporting in clinical research projects Strong understanding of healthcare compliance issues related to research projects and patient safety Join us to be part of a passionate team committed to advancing healthcare through rigorous research. Your expertise will directly impact the development of new treatments while supporting the highest standards of clinical excellence. We value your dedication to ethical research practices and offer an environment that fosters growth, collaboration, and innovation.

Pay:

$20.00 - $25.00 per hour

Experience:

Clinical research: 3 years (Preferred)

Language:

English (Preferred) Ability to

Commute:

Tampa, FL 33613 (Preferred)

Work Location:

In person