Clinical Research Coordinator at Iterative Health

Rochester, New York, United States

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Not SpecifiedCompensation

Mid-level (3 to 4 years)Experience Level

Full TimeJob Type

UnknownVisa

Healthcare, Clinical Research, GastroenterologyIndustries

Requirements

Medical Assistant or LPN required
Associates degree in a clinical or scientific-related discipline preferred
1+ years previous experience as a clinical research coordinator for pharmaceutical phase II or III trials, GI trials experience preferred
Computer skills - Microsoft Word, Excel, PowerPoint, CTMS, EMR
Previous experience in a role of complex administration or project coordination
Effective communication skills to include written, verbal, and presentation skills
Strong attention to detail and organizational, analytical, and problem-solving skills, an agile sense of prioritization and urgency
Collaborative mindset
Periodic local travel to other practice locations on an as-needed basis
Spanish speaker (Required)
Phlebotomy: 1 year (Preferred)
Physical ability to stand and walk throughout the day, prolonged periods of sitting and performing administrative duties including computer use, bend, twist, stoop, and reach, lift and carry supplies and equipment up to 15 pounds

Responsibilities

Administratively and clinically manage industry-sponsored clinical trials
Adhere to Research SOP’s, Good Clinical Practices, and the study protocols
Participate actively in communication of status and results to senior management
Assist in training site personnel in regulatory, lab procedures, and general study-related training
Assist in patient recruitment by performing detailed chart reviews and patient interviews
Discuss study protocols with patients and verify the informed consent documentation
Review medical history of patients against Inclusion/Exclusion Criteria of studies
Perform blood draws, process and ship blood/urine specimens per study 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, ensuring data integrity and consistency with prescribed study protocol
Ensure the filing and maintenance of all regulatory documents
Schedule and prepare for monitor visits
Complete and maintain case report forms per FDA guidelines, and review them against the patient’s medical record for completeness and accuracy
Maintain contact with clients and resolve any issues or questions for which the client made inquiries
Assist with Practice focus on improving patient satisfaction and the patient experience
Assist in preparing a brief monthly report on key indicators and issues

Skills

Key technologies and capabilities for this role

Good Clinical PracticesGCPClinical TrialsPatient RecruitmentInformed ConsentBlood DrawsECGVital SignsIATA RegulationsRegulatory DocumentsCase Report FormsFDA GuidelinesData VerificationChart Reviews

Questions & Answers

Common questions about this position

What qualifications are required for the Clinical Research Coordinator role?

A Medical Assistant or LPN certification is required, with an Associates degree in a clinical or scientific-related discipline preferred. Candidates need 1+ years of experience as a clinical research coordinator for pharmaceutical phase II or III trials, preferably in GI trials, along with computer skills in Microsoft Word, Excel, PowerPoint, CTMS, and EMR.

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

This information is not specified in the job description.

What is the salary or compensation for this role?

This information is not specified in the job description.

What key skills make a strong candidate for this position?

Strong candidates will have effective communication skills including written, verbal, and presentation skills, strong attention to detail, organizational, analytical, and problem-solving skills, an agile sense of prioritization and urgency, and a collaborative mindset.

Does the role involve any travel?

The position requires periodic local travel.

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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