Clinical Research Coordinator

Company Description

West Broward Rheumatology Associates is a healthcare practice dedicated to providing high-quality care for patients with rheumatic diseases and arthritis. Located in Fort Lauderdale, FL, the practice combines compassionate patient care with a commitment to medical research. By conducting clinical trials, the team strives to advance treatments and improve patient outcomes.

Role Description

This is a full-time on site role for a Clinical Research Coordinator based in Fort Lauderdale, FL. The Clinical Research Coordinator will ensure proper protocol implementation, and maintain compliance with regulatory requirements. Responsibilities include obtaining informed consent from participants, conducting study-related activities, managing data collection, and collaborating with teammates to ensure the success of ongoing projects.

Join our dynamic team as a Clinical Research Coordinator and play a vital role in advancing medical science through the management of clinical trials. This position offers an exciting opportunity to oversee study activities, ensure compliance with regulatory standards, and contribute to innovative research that impacts patient care worldwide. You will coordinate all aspects of clinical studies, from participant recruitment to data collection, fostering a collaborative environment that promotes excellence and integrity in clinical research.

Responsibilities

• Ensuring adherence to protocols, FDA regulations, and ICH Good Clinical Practice (GCP) standards
• Coordinate participant recruitment, screening, enrollment, and retention while maintaining detailed documentation in electronic medical record (EMR) systems
• Monitor patient safety by conducting vital signs assessments, blood sampling, phlebotomy procedures, and tracking adverse events in compliance with study protocols
• Review and verify clinical trial documentation for accuracy, completeness, and regulatory compliance
• Oversee data collection and analysis using statistical software and ensure adherence to CDISC standards for data formatting and reporting
• Collaborate with multidisciplinary teams to facilitate smooth trial operations
• Ensure confidentiality and compliance with HIPAA regulations during all patient interactions and data handling activities

Experience

• Proven experience in clinical trials or research projects
• Strong understanding of medical terminology, clinical laboratory procedures, and blood sampling techniques
• Experience with EMR systems and data management tools used in clinical research environments
• Familiarity with FDA regulations, ICH GCP guidelines, HIPAA compliance, and clinical development processes
• Background in healthcare field is highly desirable

Embark on a rewarding career where your expertise directly contributes to groundbreaking health advancements. Join us to make a meaningful difference in patient outcomes through meticulous study coordination and innovative research practices.

Pay: $26.19 - $31.54 per hour

Benefits:

• 401(k) matching
• Dental insurance
• Health insurance
• Life insurance
• Paid time off
• Vision insurance

Experience:

• Clinical research: 1 year (Required)

Ability to Commute:

• Tamarac, FL 33321 (Required)

Work Location: In person