Clinical Research Coordinator I — Drive Innovative Trials

Socket.dev; Cordova (TN); On-site; USD 55,000 - 75,000; Full time

Job summary

Iterative Health is seeking a Clinical Research Coordinator I to help drive successful clinical trials and ensure patient safety and data integrity across studies. You will work with sponsors, CROs, investigators, and internal teams to support study activities, enrollment, and documentation.

You will coordinate visits, collect samples, review charts, and assist with protocol adherence and compliance with GCP/HIPAA guidelines. This is a hands-on role focused on quality patient experiences.

Qualifications

• Associate’s or Bachelor’s degree in a scientific, healthcare, or related discipline required.
• 1–3 years of clinical research or healthcare experience required.
• Must be able to perform blood draw, medical review (blood pressure, height, weight etc.) & EKGs, as applicable by state law
• Strong organizational skills and attention to detail
• Ability to manage competing priorities in a fast‑paced environment
• Ability to read, interpret, and apply research protocols and clinic policies
• Proficiency with standard office software and willingness to learn clinical research systems
• Familiarity with CTMS or EDC systems preferred

Responsibilities

• 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
• Maintain accurate and timely study documentation including source records, informed consent forms, CTMS updates, and case report forms
• Maintain ongoing communication with sponsors, CROs, investigators, and internal site teams to support study execution

Skills

Clinical research

Blood draws

EKGs

CTMS

EDC

Organizational skills

Attention to detail

Education

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

Tools

CTMS

EDC

Microsoft Office

Job description

Iterative Health is seeking a Clinical Research Coordinator I to help drive successful clinical trials and ensure patient safety and data integrity across studies. You will work with sponsors, CROs, investigators, and internal teams to support study activities, enrollment, and documentation.

You will coordinate visits, collect samples, review charts, and assist with protocol adherence and compliance with GCP/HIPAA guidelines. This is a hands-on role focused on quality patient experiences.