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Iterative HealthPosted 28 days ago

Clinical Research Coordinator I

Full-time
On-site
1–3 years
Competitive
Posted 28 days ago

Iterative Health is a healthcare technology and services company accelerating clinical research to improve patient outcomes. The Clinical Research Coordinator I supports the day-to-day execution of clinical trials, coordinating patient visits, recruitment, documentation, procedures, data entry, and communications while ensuring protocol, regulatory, and patient safety compliance.

Posted
28 days ago
Source
linkedin.com
Sector
Healthcare

Opens the employer's application page in a new tab

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

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
  • 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

Preferred

  • Familiarity with CTMS or EDC systems preferred

Required skills

Clinical ResearchBlood DrawVital Signs AssessmentElectrocardiography (EKG)Research ProtocolsClinical Practice (GCP)HIPAA ComplianceInformed Consent CoordinationLaboratory Specimen Processing

Nice to have

Cambridge, Massachusetts, USAhttps://iterative.healthGrowth StageTotal Funding$268.6MKey InvestorsObvious Ventures2026-04-30Series C· $77M2022-01-19Series B· $150M2021-08-03Series A· $30MLeadership Team

Full job description

Iterative Health is a healthcare technology and services company accelerating clinical research to improve patient outcomes. The Clinical Research Coordinator I supports the day-to-day execution of clinical trials, coordinating patient visits, recruitment, documentation, procedures, data entry, and communications while ensuring protocol, regulatory, and patient safety compliance.

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

Required skills

  • Clinical Research, Blood Draw, Vital Signs Assessment, Electrocardiography (EKG), Research Protocols, Clinical Practice (GCP), HIPAA Compliance, Clinical Trial Management Systems (CTMS), Electronic Data Capture (EDC) Systems, Informed Consent Coordination, Laboratory Specimen Processing, Investigational Product Accountability

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

  • 1-3 years

Job details

Employment type

Full-time

Seniority level

1–3 years

Date posted

Oct 16, 2026

Work mode

On-site

Job source

linkedin.com

Company

Iterative Health

Healthcare

Clinical research technology and services for accelerating novel therapies

See all 12 jobs from Iterative Health →
  • Cambridge, Massachusetts, USA
  • Healthcare
  • 51-200 employees
  • Founded 2017
  • iterative.health

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