GI Clinical Research RN Coordinator

Seae Ventures

City of Rochester (NY)

On-site

USD 43,000 - 62,000

Full time

9 days ago

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Job summary

Iterative Health, a healthcare technology and services company, is seeking a Clinical Research Coordinator I – RN to support and coordinate daily clinical trial activities across its network. The role emphasizes patient interactions, data integrity, protocol compliance, and efficient trial operations.

The ideal candidate will have an active RN license, 1–2 years of clinical research experience, strong communication, and the ability to work in a fast-paced, protocol-driven environment with

Qualifications

  • Active RN license required.
  • 1–2 years of clinical research experience preferred.
  • Solid nursing background with GI focus preferred.
  • Strong written and verbal communication skills.
  • Highly organized with ability to manage multiple priorities and meet deadlines.
  • Proficiency in CTMS and standard office software.

Responsibilities

  • Administratively and clinically manage industry-sponsored clinical trials, including protocol management and patient interactions.
  • Schedule patient visits and procedures per protocol.
  • Enter study data into CTMS regularly and maintain study documentation.
  • Lead patient recruitment activities and obtain informed consent.
  • Perform clinical procedures per protocol and site policies (vital signs, blood draws, ECGs, IV administration as applicable).
  • Maintain compliance with GCP and regulatory requirements, and protect participant rights and safety.

Skills

RN license
Clinical research experience
GI specialty knowledge
Strong communication
Organizational skills
CTMS proficiency
Independent work

Education

RN licensure or BSN

Tools

CTMS platforms
Office software

Job description

Iterative Health, a healthcare technology and services company, is seeking a Clinical Research Coordinator I – RN to support and coordinate daily clinical trial activities across its network. The role emphasizes patient interactions, data integrity, protocol compliance, and efficient trial operations.

The ideal candidate will have an active RN license, 1–2 years of clinical research experience, strong communication, and the ability to work in a fast-paced, protocol-driven environment with

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