Clinical Research Coordinator

Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 70+ clinical research sites across US and Europe accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies. Our focus is on driving the success and growth of our partner sites by empowering them with tech-enabled services. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.

Company Conformance Statements

In the performance of their respective tasks and duties all employees are expected to conform to

the following :

• Perform quality work within deadlines with or without direct supervision.
• Interact professionally with other employees, customers and suppliers.
• Work effectively as a team contributor on all assignments.
• Work independently while understanding the necessity for communicating and

coordinating work efforts with other employees and organizations.

Position purpose

The Clinical Research Coordinator (CRC) is a specialized research professional working with

and under the direction of the Director and Clinical Principal Investigator (PI). The CRC

supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in

the conduct of the study.

Responsibilities / Duties / Functions / Tasks :

and IRB requirements and approvals.

Management System to ensure billing to appropriate funding source.

drugs / devices, follows the sponsor protocol and / or Impact Research Policy on

Investigational Drug / Device Accountability.

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.

Director and PI during the course of the study.

and protocol management.

Clinical Practice guidelines or for the contracted length of time, whichever is longer.

accordance with Federal regulations

access, use, and disclosure of PHI and reports instances of noncompliance to the

appropriate compliance office.

Qualifications

Education : High school diploma / GED certificate required. Associates degree from an

accredited university preferred.

Experience : Minimum 1-2 years of clinical research experience.

Other Requirements : None

Performance Requirements :

appropriate practice management software.

Equipment Operated : Standard office equipment including computers, fax machines, copiers,

printers, telephones, etc.

Work Environment : Position is in a well-lighted medical office environment. Occasional

evening and weekend work.

Physical Requirements : Must possess the physical and mental abilities to perform tasks such as

sitting for 90 percent of the day; manual dexterity to operate office machines including computer

and calculator; stooping, bending to handle files and supplies; and mobility to complete errands

or deliveries. Stress can be triggered by multiple staff demands and deadlines.

At Iterative Health, we're actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.