Clinical Research Coordinator I - Start in Trials

Socket.dev; Southaven (MS); On-site; USD 50,000 - 70,000; Full time

Job summary

Iterative Health is seeking a Clinical Research Coordinator I to support the execution of clinical trials and enhance the patient research experience. You will assist with day-to-day study activities, ensure protocol compliance, and protect patient safety across multiple stakeholders.

You will work with sponsors, CROs, investigators, and internal teams to deliver high-quality research, coordinate visits and procedures, assist recruitment efforts, and help maintain study documentation and data

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.

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 compliance with GCP guidelines and site SOPs.
• Maintain accurate and timely study documentation including source records, CRFs, and CTMS updates.
• Ensure high-quality data entry and timely resolution of data queries.
• Serve as a point of contact for study participants throughout their participation.

Skills

Clinical research experience

Healthcare experience

Education

Associate’s or Bachelor’s degree in a scientific, healthcare, or related discipline

Job description

Iterative Health is seeking a Clinical Research Coordinator I to support the execution of clinical trials and enhance the patient research experience. You will assist with day-to-day study activities, ensure protocol compliance, and protect patient safety across multiple stakeholders.

You will work with sponsors, CROs, investigators, and internal teams to deliver high-quality research, coordinate visits and procedures, assist recruitment efforts, and help maintain study documentation and data