Impactful Clinical Research Coordinator — Nephrology Trials

Medix™; Orange (CT); On-site; USD 55,000 - 80,000; Full time

Job summary

Medix is seeking a Clinical Research Coordinator to support investigational drug studies in Connecticut. You will coordinate participant care from screening to completion, ensure proper informed consent, and maintain source records with strict adherence to GCP and HIPAA standards.

The role requires 3+ years of CRC experience in patient-facing research, with the ability to manage at least three studies concurrently, and collaboration with USRC teams to ensure protocol compliance and data

Qualifications

• 3 years minimum as CRC supporting investigational drug studies.
• Experience in patient-facing research roles (MA/EMT/Phleb) preferred.
• Ability to support at least 3 studies concurrently.

Responsibilities

• Coordinate all aspects of participant care from screening through study completion.
• Ensure informed consent is documented per 45 CFR part 46.
• Maintain and update source records and eligibility documentation.
• Report adverse events and deviations to PI, Sponsor, and IRB per 21 CFR 312.
• Educate participants on protocol, IP use, safety, and rights.
• Exchange participant information with PI and research team for safety.
• Protect participant confidentiality per HIPAA.
• Dispense and instruct on IP use per protocol and PI delegation.
• Collaborate with USRC clinical team to ensure protocol compliance.
• Data collection and entry into USRC databases and CRFs/IWRS.
• Assist in long-term storage of records per requirements.
• Prepare for site initiation meetings, monitoring, audits.
• Maintain and update Trial Master File documents (FDA forms etc).
• Coordinate internal/external resources for recruitment and enrollment goals.
• Promote patient-care culture focused on safety and quality.
• Attend staff meetings and maintain reliable attendance.

Skills

CRC experience

Patient-facing role

Multiple studies

GCP familiarity

Tools

IWRS

GCP knowledge

Job description

Medix is seeking a Clinical Research Coordinator to support investigational drug studies in Connecticut. You will coordinate participant care from screening to completion, ensure proper informed consent, and maintain source records with strict adherence to GCP and HIPAA standards.

The role requires 3+ years of CRC experience in patient-facing research, with the ability to manage at least three studies concurrently, and collaboration with USRC teams to ensure protocol compliance and data