Clinical Research Coordinator at Iterative Health

Cordova, Tennessee, United States

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Not SpecifiedCompensation

Junior (1 to 2 years)Experience Level

Full TimeJob Type

UnknownVisa

Healthcare, Clinical ResearchIndustries

Requirements

Adherence to Research SOP’s, Good Clinical Practices (GCPs), study protocols, FDA guidelines, and regulatory requirements including IATA regulations for specimen shipping
Knowledge of principles of good clinical practices (GCPs) and adequate human subject protection (HSP)
Ability to perform clinical procedures including blood draws, phlebotomy, processing and shipping blood/urine specimens, dispensing study medication, collecting vital signs, and performing ECGs
Skills in patient recruitment through detailed chart reviews and patient interviews
Capability to discuss study protocols with patients and verify informed consent documentation
Proficiency in reviewing medical history against inclusion/exclusion criteria
Competence in scheduling patient research visits and procedures, data verification, quality control, and completing/maintaining case report forms
Non-exempt FLSA status with no supervisory responsibilities

Responsibilities

Administratively and clinically manage industry-sponsored clinical trials
Assist in patient recruitment by performing 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 and quality control to ensure data integrity and consistency with protocol
Complete and maintain case report forms per FDA guidelines and review against patient medical records
Function in a clinical role by conducting clinical research studies
Monitor patients and provide information to medical staff 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 for lab work and complete necessary forms
Educate patients on disease processes and clinical studies
Plan and coordinate initiation of research study protocols, operating policies, and procedures
Assist principal investigator and research director with administrative tasks for research 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 Trials ManagementPatient RecruitmentInformed ConsentChart ReviewPhlebotomyIATA ShippingECGVital SignsStudy Protocol 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 are the key responsibilities of the Clinical Research Coordinator?

Key responsibilities include administratively and clinically managing industry-sponsored clinical trials, adhering to Research SOPs, Good Clinical Practices, and study protocols, assisting in patient recruitment, performing blood draws, scheduling visits, dispensing study medication, and maintaining compliance with regulatory guidelines.

What is the salary or compensation for this role?

This information is not specified in the job description.

Does this role involve any supervisory responsibilities?

No, this position has no supervisory responsibilities.

What skills or experience make a strong candidate for this position?

Strong candidates will have experience in clinical research, knowledge of Good Clinical Practices (GCPs), ability to perform phlebotomy and blood draws, skills in patient recruitment and informed consent processes, and familiarity with regulatory compliance and study protocols.

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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