Clinical Research Coordinator (CRC)

Job Description

Opportunity to join one of the fastest-growing Clinical Research site networks in the US! The Kendall (Miami) site started in respiratory and sleep trials but has since expanded into neuroscience and infectious disease studies. Join a site that prides itself on patient care, resulting in some of the best retention rates in the industry!

Highlights

Play a major role in advancing medicine with a team dedicated to the patient experience!

Full Benefits (Health, Dental, Vision, 401k w/ 4% Match, 15 days of PTO, 10 Paid Holidays)

Competitive Base Salary

Gain experience in the fast-growing world of clinical research and develop skills that are in high demand

Monday - Friday 8:30 AM - 5 PM with some flexibility to meet patient schedules

The company is invested in growth, providing employees with unique opportunities for career advancement

Join a dedicated team at a large site with opportunities for advancement at the site and site network level.

Position

The Clinical Research Coordinator (CRC) is central to conducting and managing clinical trials, tasked with obtaining informed consent, executing study protocols, handling human specimens, and ensuring meticulous documentation and communication. This role demands a blend of precision, organization, and professional integrity, underscored by a deep commitment to providing an exceptional patient experience throughout the research journey. By fostering clear communication, demonstrating empathy, and ensuring participants feel respected and valued, CRCs play a vital role in enhancing participant engagement and adherence to study protocols.

Company

Our client is a Clinical Research site network with over 17 research sites across the United States. Their sites conduct Phase I-IV trials in therapeutic areas like cardiology, metabolic disorders, renal, CNS, pulmonology, women's health, and vaccines. They are a fast-growing site network with plans to grow from 17 sites to over 30 sites in 2024 alone.

Qualifications

Bachelor's degree preferred, but not required

Phlebotomy experience is required, EKG or other patient labs/processes preferred

Preferably 2+ years of experience as a Clinical Research Coordinator

Familiar with e-source reporting via an electronic platform

A clear understanding of ICH, FDA, and GCP regulations

Impeccable organizational skills and attention to detail

Excellent communication and interpersonal skills to effectively interact with the Principal Investigator, research team, Study Sponsor/CROs, potential subjects, and referral sources

An ethical compass that compels the candidate to be honest, detail-oriented, and self-driven

High-level critical thinking skills

Working knowledge of medical terminology and lab collection/processing/storage procedures

Proficiency with computers and Microsoft Office Suite