Back to jobs New Clinical Research Coordinator Tyler, Texas Apply 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. Job description
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
Computer skills - Microsoft Word, Excel, Power Point, 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
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.
Work Location: In person
Some of our benefits include:
Vision/Dental/ Medical Insurance
Life/Disability Insurance
Parental Leave
Stock Options
Flexible Work Hours
Unlimited Paid Time Off
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