Clinical Research Coordinator

Job Title: Clinical Research Coordinator

Work Location: Hillsborough County, Florida

Summary:

Seeking a Clinical Research Coordinator to oversee and manage clinical trials, ensuring adherence to protocols and regulatory standards. The role involves direct participant interaction, data management, and collaboration with research teams to support the advancement of medical science and patient care.

Responsibilities:

• Coordinate and manage all aspects of clinical trials, ensuring compliance with study protocols and regulatory requirements.
• Obtain and document informed consent from study participants, ensuring thorough understanding of study procedures.
• Assist with the implementation of study protocols and maintain accurate, up-to-date documentation throughout the trial.
• Schedule and coordinate patient visits, follow-ups, and related trial activities to ensure smooth study progression.
• Manage data collection processes, ensuring accuracy and integrity of clinical trial data.
• Collaborate with research teams and sponsors to facilitate effective communication and trial execution.
• Monitor participant safety and address any issues or concerns in accordance with ethical and regulatory standards.
• Support patient recruitment efforts and contribute to the overall success of clinical research initiatives.

Qualifications:

• Proficiency in administering and documenting informed consent processes, ensuring participant understanding of study protocols.
• Strong familiarity with research methodologies, clinical protocols, and study implementation procedures.
• Experience in clinical research and expertise in managing clinical trials.
• Attention to detail, strong organizational skills, and ability to manage multiple tasks with precision.
• Excellent communication and interpersonal skills for participant interaction and team collaboration.
• Bachelor’s degree in a relevant field or equivalent experience preferred.
• Certification as a Clinical Research Coordinator (CCRC) or similar is a plus.
• Familiarity with Good Clinical Practice (GCP) guidelines and FDA regulations.
• Proficiency in English and Spanish required.

Published Category: Clinical Operations & Development