Clinical Research Coordinator I - Fast-Paced Trials

Iterative Health; Providence (RI); On-site; USD 55,000 - 75,000; Full time

Job summary

Iterative Health in Providence, RI seeks a Clinical Research Coordinator I to support day-to-day trial activities, ensure protocol and regulatory compliance, and deliver a positive participant experience.

You’ll partner with sponsors, CROs, investigators and internal teams to coordinate visits, collect data, and help recruitment, while maintaining accurate documentation and patient safety standards.

Qualifications

• 1–3 years of clinical research or healthcare experience.
• Ability to perform blood draws and cardiovascular measurements.
• Familiarity with CTMS or EDC systems preferred.

Responsibilities

• Support the coordination and execution of industry-sponsored clinical trials under the guidance of site leadership and senior research staff.
• Coordinate patient visits, procedures, and study-related activities in accordance with protocol requirements and study timelines.
• Support patient recruitment and retention activities including chart review, patient outreach, scheduling, and informed consent coordination.
• 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, and investigational product accountability, as permitted by applicable regulations, training, and organizational policy.
• Process laboratory specimens and prepare shipments in accordance with protocol requirements and applicable IATA regulations.
• Maintain accurate and timely study documentation including source records, informed consent forms, CTMS updates, and case report forms.
• Ensure high-quality data entry and support timely resolution of data queries.
• Serve as a point of contact for study participants throughout study participation.
• Maintain ongoing communication with sponsors, CROs, investigators, and internal site teams to support study execution.
• Support preparation for sponsor, CRO, and regulatory monitoring visits.
• Maintain inventory and organization of study equipment, supplies, and investigational products.
• Support the protection of human research participants in compliance with federal regulations, GCP, HIPAA, and institutional policies.
• Maintain compliance with all site SOPs, privacy standards, and research protocols.
• Perform job related duties as requested.

Skills

Clinical research experience

Organizational skills

Reading protocols

CTMS/EDC familiarity

Office software proficiency

Blood draw/ECG ability

Education

Associate's or Bachelor's degree in a scientific/healthcare field

Tools

CTMS/EDC systems

Job description

Iterative Health in Providence, RI seeks a Clinical Research Coordinator I to support day-to-day trial activities, ensure protocol and regulatory compliance, and deliver a positive participant experience.

You’ll partner with sponsors, CROs, investigators and internal teams to coordinate visits, collect data, and help recruitment, while maintaining accurate documentation and patient safety standards.