Clinical Research Coordinator II

Iterative Health is hiring a Clinical Research Coordinator II to independently coordinate clinical trials from start-up through closeout, ensuring protocol compliance, regulatory standards, and patient safety. The role manages study activities, patient recruitment and retention, documentation and data quality, and communication with participants, investigators, sponsors, and CROs.

Responsibilities

Independently coordinate and manage industry-sponsored clinical trials from study start-up through closeout with minimal supervision

Manage complex study visit schedules and protocol-related activities while ensuring adherence to study timelines and requirements

Lead patient recruitment and retention efforts including chart review, patient outreach, informed consent discussions, and enrollment tracking to support study enrollment goals

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, investigational product accountability, and phlebotomy, 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, complete, and timely study documentation including source records, informed consent forms, CTMS updates, and case report forms

Ensure high-quality data entry and timely resolution of data queries in accordance with sponsor expectations and established timelines

Serve as a primary point of contact for study participants throughout study participation

Maintain ongoing communication with sponsors, CROs, investigators, site leadership, and internal teams to proactively resolve study-related issues

Prepare for and support sponsor, CRO, and regulatory monitoring visits, audits, and inspections

Review safety reports and ensure appropriate investigator review and documentation in a timely manner

Maintain inventory and organization of study equipment, supplies, and investigational products onsite

Contribute to process improvement initiatives to enhance site performance, operational efficiency, and patient experience

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

May support onboarding and mentorship of junior research staff and coordinators

Perform job related duties as requested

Preferred

Experience in [gastroenterology, hepatology, cardiology] therapeutic areas preferred

CCRC® — Certified Clinical Research Coordinator or CCRP® — Certified Clinical Research Professional or equivalent clinical research certification preferred

Familiarity with CTMS or EDC systems preferred

Gastroenterology experience

Hepatology experience

Cardiology experience

CCRC certification

CCRP certification

Clinical research certification

CTMS familiarity

EDC system familiarity

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

3-5 years of clinical research or healthcare experience required

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 CTMS, EDC systems, and standard office software applications

Experience in [gastroenterology, hepatology, cardiology] therapeutic areas preferred

CCRC® — Certified Clinical Research Coordinator or CCRP® — Certified Clinical Research Professional or equivalent clinical research certification preferred

Familiarity with CTMS or EDC systems preferred

Required skills

Clinical Research, CTMS, EDC, Gastroenterology, Hepatology, Cardiology, CCRC Certification, CCRP Certification, Research Protocol Interpretation

Preferred skills

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

Experience

3-5 years