Job Description

Clinical Research Coordinator

Location: Miami, FL

Employment Type: Full-time, On-site

Company Description

Research Associates of South Florida is a premier medical research facility committed to advancing medicine and providing exceptional care across various specialties. With a team of board-certified physicians and experienced research staff, we deliver groundbreaking contributions to medicine while offering cutting-edge treatments and comprehensive healthcare services.

Position Overview

We are seeking a dedicated Clinical Research Coordinator (CRC) to join our team in Miami, FL. The CRC will manage daily operations of clinical research projects, ensuring adherence to protocols, ethical standards, and regulatory requirements. This role plays a vital part in patient care and research integrity, requiring exceptional organizational and interpersonal skills.

Responsibilities

• Study Oversight : Coordinate the smooth execution of assigned clinical trials with a focus on patient recruitment, retention, and protocol adherence.
• Informed Consent : Conduct informed consent discussions, ensuring patients understand study objectives and any updates or changes to protocols or consent forms.
• Patient Interaction : Administer questionnaires, monitor patients for protocol compliance, and ensure adherence to study rules and ethical standards.
• Regulatory Compliance : Maintain detailed study records in compliance with Good Clinical Practice (GCP), ALCOA, FDA guidelines, and other regulatory standards.
• Data Management : Collect and document data accurately in source documents to support data entry teams.
• Investigational Product Management : Store, monitor, and dispense investigational products according to protocols; report temperature excursions and maintain accountability.
• Study Preparation : Ensure study supplies and equipment are in stock, functional, and inventoried as required.
• Engagement : Collaborate with study monitors and prepare for interim monitoring visits while maintaining effective communication with study subjects.
• Recordkeeping : Maintain research chart source records and manage study files to facilitate efficient study operations. We use eSource!

Qualifications

• Proficiency in informed consent processes and protocol management.
• Experience with clinical research and clinical trial coordination.
• Strong organizational and project management skills.
• Excellent communication and interpersonal abilities.
• Detail-oriented and capable of thriving in a collaborative team environment.

Why Join Us?

At Research Associates of South Florida, you’ll be part of a passionate team dedicated to advancing medical science and improving patient care. This is a unique opportunity to contribute to meaningful research in a supportive and professional environment.

Apply now to become a part of a team that’s changing lives and shaping the future of medicine!

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