Clinical Research Coordinator at Iterative Health

New Albany, Indiana, United States

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Not SpecifiedCompensation

Junior (1 to 2 years)Experience Level

Full TimeJob Type

UnknownVisa

Healthcare, Clinical Research, GastroenterologyIndustries

Requirements

Adherence to Research SOP’s, Good Clinical Practices (GCPs), study protocols, FDA guidelines, and regulatory standards
Compliance with principles of adequate human subject protection (HSP), patient safety, and confidentiality
Ability to perform clinical procedures including blood draws, phlebotomy, processing and shipping blood/urine specimens per IATA regulations, vital signs collection, ECGs, and dispensing study medication
Knowledge of informed consent processes, patient recruitment via chart reviews and interviews, and verifying inclusion/exclusion criteria
Skills in scheduling patient visits/procedures, data verification, quality control, completing/maintaining case report forms, and ensuring data integrity
Capability to monitor patients, educate staff and patients on studies/disease processes, and act as a resource on investigational issues
Understanding of clinical trial coordination from initiation to completion, including planning, staffing, data collection/analysis systems, progress monitoring, and reporting

Responsibilities

Administratively and clinically manage industry-sponsored clinical trials
Assist in patient recruitment through detailed chart reviews and patient interviews
Discuss study protocols with patients and verify informed consent documentation
Review patient medical history against inclusion/exclusion criteria
Perform blood draws, process and ship blood/urine specimens per protocol and IATA regulations
Schedule all patient research visits and procedures consistent with protocol requirements
Dispense study medication, collect vital signs, and perform ECGs
Assist with routine data verification, quality control, and maintaining case report forms per FDA guidelines
Function in a clinical role conducting research studies and monitoring patients for optimal outcomes
Develop written research study information/tools for staff education and patient recruitment
Maintain compliance with protocols and regulatory guidelines
Act as a resource for staff on investigational issues or guidelines
Coordinate availability and distribution of medications for patients
Perform phlebotomy and complete necessary forms as required
Educate patients on disease processes and clinical studies
Plan and coordinate initiation of research protocols, operating policies, and procedures
Assist principal investigator and research director with administrative tasks for study operations
Plan and coordinate staffing of research studies, including recruitment and administration of support staff
Plan, implement, and maintain data collection and analysis systems
Monitor progress of research activities, maintain records, and prepare periodic/ad hoc reports
Facilitate assigned clinical trials from start to finish
Screen participants for all studies

Skills

Key technologies and capabilities for this role

GCPClinical TrialsPatient RecruitmentChart ReviewsInformed ConsentBlood DrawsIATA RegulationsVital SignsECGStudy ProtocolsSOP Adherence

Questions & Answers

Common questions about this position

Is this position remote or does it require on-site work?

This information is not specified in the job description.

What is the salary or compensation for the Clinical Research Coordinator role?

This information is not specified in the job description.

What key skills are required for the Clinical Research Coordinator position?

Key skills include adhering to Good Clinical Practices (GCPs), performing phlebotomy and blood draws, patient recruitment through chart reviews and interviews, and managing clinical trial activities like scheduling visits, dispensing medication, and data verification.

Does this role involve any supervisory responsibilities?

No, this position has no supervisory responsibilities.

What experience or qualifications make a strong candidate for this role?

Strong candidates will have experience coordinating clinical trials, ensuring GCP compliance, performing clinical procedures like phlebotomy and ECGs, and managing patient recruitment and data integrity.

Iterative Health

AI-driven solutions for gastrointestinal care

About Iterative Health

Iterative Health focuses on improving gastrointestinal (GI) care through the use of artificial intelligence (AI) and machine learning (ML). Their main product, SKOUT®, is an FDA-cleared device designed to help doctors detect adenomas, which are precursors to colorectal cancer. This device works alongside physician judgment to enhance the accuracy of diagnoses. In addition to SKOUT®, Iterative Health provides services that optimize clinical trials by using AI-enabled documentation technology, which improves patient care and ensures high-quality reporting across different healthcare institutions. This technology aims to make advanced care more accessible, especially to underserved populations. Unlike many competitors, Iterative Health combines AI technology with a strong focus on colorectal cancer prevention and clinical trial efficiency. The company's goal is to deliver top-tier GI care and improve health outcomes for patients worldwide.

Boston, MassachusettsHeadquarters

2017Year Founded

$182.1MTotal Funding

SERIES_BCompany Stage

AI & Machine Learning, HealthcareIndustries

51-200Employees

Benefits

Vision/Dental/ Medical Insurance

Life/Disability Insurance

Parental Leave

Stock Options

Flexible Work Hours

Unlimited Paid Time Off

Risks

Competition from tech giants in AI medical imaging threatens Iterative Health's market share.

Rapid expansion and partnerships may strain operational capabilities and resources.

Reliance on AI exposes Iterative Health to potential ethical and regulatory scrutiny.

Differentiation

Iterative Health uses AI to enhance GI care, focusing on colorectal cancer prevention.

Their SKOUT® device aids in adenoma detection, improving diagnostic accuracy in endoscopy.

AI-enabled documentation technology optimizes clinical trials, enhancing research quality and continuity.

Upsides

AI-driven predictive analytics in gastroenterology allow for personalized, effective patient care.

Partnerships with Gastro Health and One GI® expand clinical research capabilities in GI care.

$150M Series B funding accelerates AI innovations, transforming gastroenterology care.

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