Clinical Research Coordinator I

Iterative Health is a healthcare technology and services company that supports clinical research across a network of research sites. The Clinical Research Coordinator I coordinates day-to-day clinical trial activities, supports patients and study teams, and helps ensure protocol compliance, accurate documentation, and patient safety.

Responsibilities

• 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

Preferred

• Familiarity with CTMS or EDC systems preferred
• CTMS
• EDC Systems

Company

• Clinical research technology and services for accelerating novel therapies
• Cambridge, Massachusetts, USA
• https://iterative.health/
• Founded in 2017
• 51-200 employees

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

Required skills

• Clinical Research, Clinical Trial Management Systems (CTMS), Electrocardiograms (EKGs), Electronic Data Capture (EDC), Phlebotomy, Research Protocol Interpretation, Vital Signs Assessment

Preferred skills

• $268.6M, 2021-08-03, 2022-01-19, 2026-04-30, 2026-05-14, 2026-07-10, 2026-08-11, AI Tools, Aditya Khosla, Business Wire, CEO, CTO & Board Member, Cambridge, Massachusetts, USA, Clearlake Capital Group,Insight Partners, Company data provided by, Customize Your Resume, Familiarity with CTMS or EDC systems preferred, Google Ventures,Intrepid Growth Partners, Growth Stage, Jonathan Ng, Key Investors, Leadership Team, Maximize your interview chances, Obvious Ventures, Recent News, Series A· $30M, Series B· $150M, Series C· $77M, Total Funding, https://iterative.health

Experience

• 1-3 years