Clinical Research Coordinator I — Patient-Centric Trials Lead

Iterative Health; Houston (TX); On-site; USD 52,000 - 76,000; Full time

Job summary

Iterative Health is seeking a full-time Clinical Research Coordinator to support and coordinate daily clinical trial activities within our healthcare technology environment.

The role includes patient recruitment, scheduling visits, performing visits and data handling while ensuring compliance with SOPs and FDA guidelines. Open to relocation; strong communication and clinical research experience preferred.

Qualifications

• Minimum 1-2 years of clinical research experience
• Medical Assistant, LPN, or similar health credential preferred
• Strong written and verbal communication skills
• Ability to read, interpret, and apply clinic policies and protocols
• Proficient with standard office software (e.g., MS Office)
• Ability to lift up to 25 pounds

Responsibilities

• Manage industry-sponsored clinical trials administratively and clinically
• Lead patient recruitment activities and verify informed consent documentation
• Schedule patient visits and procedures per study protocol
• Conduct patient visits and collect vital signs/ECGs as required
• Perform blood draws, process/shipping of specimens per protocol and IATA rules
• Maintain study documentation, source docs, consents and CRFs in CTMS
• Serve as primary contact for study participants and ensure regulatory compliance

Skills

Clinical research

Communication skills

Data entry

Team collaboration

Problem solving

Education

Bachelor's degree in clinical/science field

Associate degree in health field / Medical Assistant or Nursing

Job description

Iterative Health is seeking a full-time Clinical Research Coordinator to support and coordinate daily clinical trial activities within our healthcare technology environment.

The role includes patient recruitment, scheduling visits, performing visits and data handling while ensuring compliance with SOPs and FDA guidelines. Open to relocation; strong communication and clinical research experience preferred.