Clinical Research Coordinator at Iterative Health

Sun City, Arizona, United States

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Not SpecifiedCompensation

Junior (1 to 2 years)Experience Level

Full TimeJob Type

UnknownVisa

Healthcare, Clinical ResearchIndustries

Requirements

High school diploma/GED certificate required. Associates degree from an accredited university preferred
Minimum 1-2 years of clinical research experience
Knowledge of grammar, spelling, and punctuation
Knowledge of purchasing, budgeting, and inventory control
Skill in taking and transcribing dictation and operating office equipment
Skill in answering the phone and responding to questions
Skill in time management, prioritization, and multitasking

Responsibilities

Communicate study requirements to all individuals involved in the study
Develop and implement recruitment strategies in accordance with Impact Research and IRB requirements and approvals
Screen subjects for eligibility using protocol specific inclusion and exclusion criteria
Enter participant information and study visit procedures into the Clinical Trial Management System to ensure billing to appropriate funding source
Maintain adequate inventory of study supplies. When handling investigational drugs/devices, follow the sponsor protocol and/or Impact Research Policy on Investigational Drug/Device Accountability
Complete study documentation and maintenance of study files in accordance with sponsor requirements and Impact Research policies and procedures including, but not limited to, consent forms, source documentation, narrative notes if applicable, case report forms, and investigational material accountability forms
Maintain effective and ongoing communication with sponsor, research participants, Director and PI during the course of the study
Manage the day-to-day activities of the study including problem solving, communication and protocol management
Collect and report ongoing patient recruitment/enrollment metrics to Director and PI
Arrange secure storage of study documents that will be maintained according to Good Clinical Practice guidelines or for the contracted length of time, whichever is longer
Protect the rights and welfare of all human research participants involved in research in accordance with Federal regulations
Cooperate with Impact Research compliance and monitoring efforts regarding the access, use, and disclosure of PHI and report instances of noncompliance to the appropriate compliance office
Other duties as assigned

Skills

Key technologies and capabilities for this role

Clinical TrialsIRBPatient RecruitmentEligibility ScreeningCTMSProtocol Compliance

Questions & Answers

Common questions about this position

What are the main responsibilities of the Clinical Research Coordinator?

The CRC supports, facilitates, and coordinates daily clinical trial activities, including communicating study requirements, screening subjects, managing study documentation, maintaining inventory, and ensuring effective communication with sponsors, participants, Director, and PI.

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 this role?

This information is not specified in the job description.

What does the company expect from employees in terms of work style?

Employees are expected to perform quality work within deadlines with or without direct supervision, interact professionally, work effectively as a team contributor, and work independently while communicating and coordinating efforts.

What makes a strong candidate for the Clinical Research Coordinator position?

A strong candidate should have experience in clinical trials, strong organizational skills for managing study activities and documentation, effective communication abilities, and the capacity to work independently and as a team under the direction of the Director and PI.

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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