Clinical Research Coordinator

Iterative Health is a healthcare technology and services company on a mission to advance gastrointestinal care through relentless innovation. With deep expertise in artificial intelligence and clinical research we empower healthcare professionals to provide consistently high-quality colorectal cancer screenings and support clinical research teams and study sponsors to expand and accelerate patient access to novel therapeutics.

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 Site Manager and 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:

• Regular communication of study requirements and changes to relevant members of study staff Implement recruitment strategies in order to prescreen screen and enroll subjects in active trials Screen subjects for eligibility using protocol specific inclusion and exclusion criteria documenting each potential participants eligibility or exclusion.
• Acts as a point of reference for study participants by answering questions and keeping them informed of study progress

General Business

• Ensure relevant study and subject specific information is entered into the CTMS system on a regular basis. Maintains adequate inventory of study equipment and supplies onsite at all times. .
• Conducts patient visits as outlined within each study protocol.
• Complete study documentation and maintenance of study files including but not limited to consent forms source documentation progress notes if applicable case report forms and investigational accountability forms.
• Maintains ongoing communication with the CRO sponsor research participants Site Manager and PI throughout course of the study.
• Manage the day to day activities of the study including problem solving communication and protocol management.
• Ensure all safety data is reviewed by the PI in a timely manner.
• Protects the rights and welfare of all human research participants involved in research Other duties as assigned.

Qualifications

Education: Bachelors Degree preferred

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

Other Requirements: None

Performance Requirements:

• 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.
• Skill in writing and communicating effectively.
• Ability to work under pressure communicate and present information. Ability to read interpret and apply clinic policies and procedures.
• Ability to identify problems recommend solutions organize and analyze information. Ability to multi-task establish priorities and coordinate work activities. Ability to competently use Microsoft Office including Word PowerPoint Excel and 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.

General Business

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.

Some of our benefits include:

• Vision/Dental/ Medical Insurance
• Life/Disability Insurance
• Parental Leave
• Stock Options
• Flexible Work Hours
• Unlimited Paid Time Off

At Iterative Health were 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