Clinical Research Coordinator

Research Associates of South Florida; Miami (FL); On-site; USD 60,000 - 80,000; Full time

Job summary

A healthcare organization in Miami is seeking a Clinical Research Coordinator to oversee daily operations of clinical trials. The ideal candidate will be responsible for managing study protocols, obtaining informed consent, and ensuring compliance with ethical guidelines. The candidate should possess strong organizational skills and strong clinical research experience. This is a full-time, on-site position offering the opportunity to contribute to advancements in medicine.

Qualifications

• Proficiency in obtaining Informed Consent and ensuring participants' understanding.
• Experience in implementing study protocols and conducting clinical trials.
• Knowledge of regulatory and ethical considerations in clinical research.

Responsibilities

• Oversee daily operations of clinical trials.
• Manage study protocols and coordinate with investigators.
• Ensure accurate documentation and compliance with guidelines.

Skills

Obtaining Informed Consent

Clinical Research Experience

Attention to detail

Excellent interpersonal skills

Organizational skills

Education

Bachelor's degree in healthcare, science, or a related field

Job description

Research Associates of South Florida is dedicated to advancing medicine and delivering exceptional patient care across a wide range of medical specialties. Supported by a team of experienced board-certified physicians and skilled research professionals, the organization focuses on innovative contributions to the field of medicine. Committed to providing comprehensive healthcare services, it also offers access to cutting-edge treatments. Research Associates of South Florida thrives on fostering a positive impact on patient health and medical advancements.

Role Description

This is a full-time, on-site role based in Miami, FL, for a Clinical Research Coordinator. The Clinical Research Coordinator will oversee the daily operations of clinical trials, including managing study protocols, coordinating with investigators and staff, and ensuring accurate documentation. Responsibilities include obtaining informed consent, monitoring patient progress, preparing reports, and ensuring compliance with regulatory and ethical guidelines.

Qualifications

• Proficiency in obtaining Informed Consent and ensuring participants' understanding and compliance
• Experience in implementing and adhering to study Protocols and conducting Clinical Trials
• Strong Clinical Research Experience and a solid understanding of research methodologies
• Attention to detail, strong organizational skills, and the ability to manage multiple tasks effectively
• Excellent interpersonal and communication skills for working collaboratively with diverse patient populations and research teams
• Knowledge of regulatory and ethical considerations in clinical research
• Bachelor's degree in healthcare, science, or a related field is preferred