Clinical Research Coordinator New Tyler, Texas

Iterative Scopes, Inc; Mississippi; On-site; USD 50,000 - 70,000; Full time

Job summary

A leading healthcare technology company is seeking a full-time Clinical Research Coordinator to manage gastrointestinal clinical research studies. Responsibilities include overseeing clinical trials, ensuring protocol adherence, and facilitating patient recruitment. Ideal candidates will have a background in nursing or clinical research, with strong communication and organizational skills.

Benefits

Vision/Dental/Medical Insurance

Life and Disability Insurance

Stock Options

Flexible Work Hours

Unlimited Paid Time Off

Qualifications

• 1+ years of experience as a clinical research coordinator.
• Experience with pharmaceutical phase II or III trials preferred.
• Effective verbal and written communication skills.

Responsibilities

• Manage industry-sponsored clinical trials and communicate findings.
• Conduct patient recruitment and ensure informed consent.
• Maintain regulatory documents and assist in data verification.

Skills

Communication

Attention to detail

Problem solving

Organizational skills

Education

Medical Assistant or LPN certification

Associates degree in clinical or scientific discipline

Bachelor's degree in Nursing

Job description

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.

We are seeking a full-time, experienced Clinical Research Coordinator. The Research Coordinator will facilitate all facets of gastrointestinal clinical research studies.

Responsibilities:

• Administratively and clinically manage industry-sponsored clinical trials
• Adhere to Research SOP’s, Good Clinical Practices and the study protocols
• Participate actively in the 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 the 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 perform procedures consistent with protocol requirements (Dispense study medication, collect vital signs and perform ECGs, etc)
• 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 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
• Assist with Practice focus on improving patient satisfaction and the patient experience
• Assist in preparing a brief monthly report on key indicators and issues

Qualifications

• 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
• 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
• Periodic local travel to other practice locations on an as-needed basis

Physical Requirements

• Ability to stand and walk throughout the day
• Prolonged periods of sitting and performing administrative duties, including the use of computers
• Ability to bend, twist, stoop, and reach
• Able to lift and carry supplies and equipment as needed (up to 15 pounds)

Job Type: Full-time

Schedule:

• Full Time
• Monday to Friday

Education:

• High school or equivalent (Preferred)
• Associate/Bachelors of Nursing, or LPN preferred.

Experience:

• 1 plus year in nursing preferred.

Some of our benefits include:

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

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 [e-mail].

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