You are applying for a position through Medix, a staffing agency. The actual posting represents a position at one of our clients.

Job Summary

Our client is seeking a Clinical Research Assistant responsible for supporting laboratory duties, patient recruitment, data management, study support, and regulatory compliance. The primary goal is to assist in the efficient operation and execution of clinical trials while ensuring adherence to industry regulations.

Key Responsibilities

• Perform venipuncture, process, pack, and ship samples following IATA regulations.
• Review and file laboratory results, ensuring proper documentation.
• Monitor and order study lab kits and supplies as needed and manage supply chain responsibilities for the lab.
• Proactively recruit study patients and conduct phone screenings according to protocols.
• Ensure patient consent forms are read, understood, and properly signed, and provide patients with copies of consent forms.
• Collect clinical data including chart documentation, patient histories, medications, vital signs, ECGs, and protocol-required procedures.
• Utilize Electronic Data Capture systems and ensure accurate data entry in Clinical Trial Management System (CTMS).
• Assist Clinical Research Coordinators in daily tasks, including organizing necessary documents and materials, and daily administrative duties.
• Comply with all HIPAA, CLIA, OSHA, FDA, and ICH regulations, as well as confidentiality agreements.

Medix Overview:

With over 20 years of experience connecting organizations with highly qualified professionals, Medix is a leading provider of workforce solutions for clients and candidates across the healthcare, scientific, technology, and government industries. Through our core purpose of positively impacting lives, we’re dedicated to creating opportunities for job seekers at some of the nation's top companies. As an award-winning career partner, Medix is committed to helping talent find fulfilling and meaningful work because our mission is to help you achieve yours.