Clinical Research Coordinator II — Lead Multisite Trials

Iterative Health

Rhode Island

On-site

USD 60,000 - 90,000

Full time

14 days+
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Job summary

Iterative Health is seeking a Clinical Research Coordinator II to independently coordinate daily study activities and ensure compliance with protocol requirements, regulatory standards, and patient safety guidelines.

You will manage complex study visits, lead patient recruitment, perform protocol-required visits and procedures, and maintain study documentation while collaborating with sponsors, CROs, investigators, and internal teams.

Qualifications

  • Associate’s or Bachelor’s degree in a scientific, healthcare, or related discipline required.
  • 3-5 years of clinical research or healthcare experience required.
  • Experience in gastroenterology, hepatology, or cardiology preferred.
  • CCRC® or CCRP® certification preferred.
  • Strong organizational skills and attention to detail.
  • Ability to manage competing priorities in a fast-paced environment.
  • Proficiency with CTMS, EDC systems, and standard office software applications.
  • Familiarity with CTMS or EDC systems preferred.

Responsibilities

  • Independently coordinate and manage industry-sponsored clinical trials from study start-up through closeout.
  • Lead patient recruitment and retention efforts including chart review, patient outreach, informed consent discussions, and enrollment tracking.
  • Conduct protocol-required patient visits and assessments in accordance with study protocols, GCP guidelines, and site SOPs.
  • Perform protocol-required clinical procedures including vital signs, ECGs, specimen collection, investigational product accountability, and phlebotomy, as permitted by applicable regulations, training, and organizational policy.
  • Maintain accurate, complete, and timely study documentation including source records, informed consent forms, CTMS updates, and case report forms.

Skills

Clinical research experience
Organizational skills
Prioritization abilities
CTMS proficiency
EDC systems experience

Education

Associate/Bachelor’s degree in scientific/healthcare field

Tools

CTMS
EDC systems
Office software

Job description

Iterative Health is seeking a Clinical Research Coordinator II to independently coordinate daily study activities and ensure compliance with protocol requirements, regulatory standards, and patient safety guidelines.

You will manage complex study visits, lead patient recruitment, perform protocol-required visits and procedures, and maintain study documentation while collaborating with sponsors, CROs, investigators, and internal teams.

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