Clinical Research Coordinator I Southaven, MS

Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes.

We built a leading performance-driven network of 100 sites across the US Europe India and Australia conducting research directly in the communities where care is delivered across gastrointestinal hepatology obesity and cardiology. By combining deep clinical trial expertise with cutting-edge AI we connect sponsors scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need. Today Iterative Health is headquartered in Cambridge Massachusetts and New York City with 250 employees world-wide.

As a Clinical Research Coordinator I (CRC I) at Iterative Health you will play an important role in the successful execution of clinical trials and the overall patient research experience. This role supports the coordination of day-to-day study activities while ensuring compliance with protocol requirements regulatory standards and patient safety guidelines.

The CRC I works closely with patients sponsors CROs investigators and internal teams to help deliver high-quality clinical research and contribute to the advancement of innovative therapies.

• 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

What You Bring to the Team

• Associates or Bachelors degree in a scientific healthcare or related discipline required
• 13 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

• Ability to sit stand and move throughout clinical and office environments for extended periods of time
• Ability to lift and move up to 25 pounds as needed

At Iterative Health were actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture and by extension hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you please contact