Clinical Research Coordinator

About Vital Heart & Vein

Established in 1998, Vital Heart & Vein is the largest private cardiology group in the Houston area, featuring 40 board-certified physicians specializing in cardiovascular disease, interventional cardiology, vascular and endovascular surgery, advanced heart failure, and podiatry. It offers advanced diagnostic and therapeutic services for coronary, electrophysiology, vascular, and vein conditions throughout Greater Houston including locations such as Humble, Pearland, West Houston, Beaumont, Northwest Houston, and the Texas Medical Center. The organization pioneers innovative cardiovascular treatments through active clinical research.

Position Overview

We are hiring a full-time Clinical Research Coordinator based in Humble, TX, to manage clinical trials and research studies, ensuring adherence to regulatory standards and ethical guidelines while maintaining high-quality data. This role acts as the primary contact among study participants, medical staff, and sponsors, significantly contributing to cardiovascular research advancement.

Key Responsibilities

• Lead and supervise clinical trial activities ensuring compliance with protocols and relevant regulations
• Participate in obtaining informed consent and uphold participant safety and ethical requirements
• Coordinate study visits, procedures, and follow-ups with healthcare professionals
• Accurately collect, document, and report clinical trial data in a timely manner
• Maintain regulatory documents, patient records, and electronic databases thoroughly
• Assist in the preparation of study reports, regulatory filings, and quality assurance initiatives
• Work collaboratively with physicians and research teams to enhance patient recruitment and retention

Qualifications

• Bachelor's degree in a relevant discipline is required; a Master's degree or clinical research certification (ACRP, SOCRA) is preferred
• Experience coordinating clinical trials, preferably within cardiology or vascular research settings
• Familiarity with informed consent processes, Good Clinical Practice (GCP), and regulatory compliance
• Excellent organizational skills, detail orientation, and communication abilities
• Capability to manage multiple projects simultaneously and collaborate effectively in a clinical environment

What We Provide

• Chance to be part of pioneering cardiovascular research initiatives
• Opportunities for professional development and support for continuing education
• A collaborative and supportive work culture
• Competitive remuneration and benefits package

Location and Employment Details

This is a full-time, on-site position based in Humble, TX.