Clinical Research Coordinator I — Accelerating Trials

Iterative Health; Lake Charles (LA); On-site; USD 55,000 - 75,000; Full time

Job summary

Iterative Health is seeking a full-time Clinical Research Coordinator to support and coordinate daily clinical trial activities across multiple sites. You will lead patient recruitment, schedule visits, perform study procedures, and ensure data integrity within CTMS systems while adhering to SOPs and FDA guidelines.

The role requires 1–2 years of clinical research experience, strong communication, and the ability to work with cross-functional teams in a fast-paced healthcare technology company.

Qualifications

• Minimum 1–2 years of clinical research experience.
• Ability to execute on research tasks with guidance from more experienced staff, PIs, and management.
• Strong written and verbal communication skills.
• Ability to read, interpret, and apply clinic policies and research protocols.
• Ability to use standard office software.

Responsibilities

• Administratively and clinically manage industry-sponsored clinical trials including problem solving, communication and protocol management.
• Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation
• Schedule all patient research visits and procedures consistent with protocol requirements
• Conduct patient visits as outlined within each study protocol
• Dispense study medication, collect vital signs and perform ECGs
• Perform blood draws, process and ship specimens per study protocol and IATA regulations
• Ensure relevant study and subject specific information is entered into the CTMS system on a regular basis; complete and maintain documentation study files
• Act as point of contact for study participants
• Adhere to Research SOPs, Good Clinical Practices, and the study protocols
• Maintain ongoing communication with the CRO, sponsor, research participants, Site Manager and PI throughout course of the study
• Ensure all safety data is reviewed by the PI in a timely manner
• Maintain inventory of study equipment and supplies onsite at all times
• Participate actively in communication of status and results to management
• Assist with routine data verification and quality control
• Schedule and prepare for monitor visits
• Assists Study Team in protection of the rights and welfare of all human research participants
• Cooperates with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncompliance
• Complete and maintain case report forms per FDA guidelines, and review them against the patient’s medical record for completeness and accuracy
• All employees are expected to:
• Perform quality work within deadlines with or without direct supervision
• Interact professionally with other employees, customers and suppliers
• Work effectively as a team contributor on all assignments
• Work independently while understanding the necessity for communicating and coordinating work efforts with other employees and organizations

Skills

Clinical research experience

Communication skills

Reading protocols

Office software

Lifting 25 pounds

Education

Medical Assistant

LPN

Associates or Bachelor’s degree in clinical/science

Tools

CTMS

Job description

Iterative Health is seeking a full-time Clinical Research Coordinator to support and coordinate daily clinical trial activities across multiple sites. You will lead patient recruitment, schedule visits, perform study procedures, and ensure data integrity within CTMS systems while adhering to SOPs and FDA guidelines.

The role requires 1–2 years of clinical research experience, strong communication, and the ability to work with cross-functional teams in a fast-paced healthcare technology company.