Clinical Research Coordinator - HPRC Tulsa

The University of Oklahoma•Tulsa, OK

3d•Onsite

About The Position

OU Health Stephenson Cancer Center is Oklahoma’s only National Cancer Institute (NCI)-Designated Cancer Center, and one of only 73 NCI-Designated Cancer Centers in the United States. This highly competitive accreditation ensures that our patients receive the highest standard of care and have access to the most advanced cancer treatment options. At the TSET Health Promotion Research Center and Stephenson Cancer Center, we have an exciting new job opportunity that could be right for you! The Clinical Research Coordinator – Tulsa identifies and assesses patients who may be eligible to participate in a clinical trial or research program, distributes information, acts as a clinical resource, manages data, conducts follow-up care for patients, and attends meetings pertaining to the program. Learn more about the Health Promotion Research Center (HPRC) here.

Requirements

Bachelor’s Degree, AND 12 months of clinical practice, nursing, or clinical trial or research program coordination experience.
Equivalency/Substitution: Will accept 48 months experience in lieu of Bachelor’s degree for a total of 60 months experience. OR Master’s Degree in lieu of experience.
Knowledge of clinical trial protocols.
Ability to communicate verbally and in writing.
Ability to explain the clinical trial study information to the participants.
Ability to read and follow instructions and guidelines.
Oklahoma State licensure is required for Nurses and Physician Assistants.
Basic Life Support (BLS)
Physical: Sitting for prolonged periods. Manual dexterity. Speaking and listening. Reaching, bending, standing and stooping.
Environmental: Clinic Environment. Exposure to infectious diseases.

Nice To Haves

Bachelor’s Degree in a health related, behavioral science, or biological science field.
Previous Research Coordinator or Research Assistant experience.

Responsibilities

Prepare and submit IRB applications and maintain regulatory documentation in compliance with institutional and federal requirements.
Develop and generate study recruitment materials (e.g., flyers, advertisements, scripts) in accordance with IRB and institutional guidelines.
Design, develop, and manage Online surveys (e.g., REDCap) and databases to support data collection and study workflows.
Identifies patients who may be eligible to participate in a clinical trial or research program.
Performs the initial assessment of potential patients.
Takes clinical history and completes patient data forms.
May perform a physical exam during the assessment.
Provides potential patients with study information.
Obtains informed consent forms.
Acts as a clinical resource and liaison between physicians, nurses, and laboratory personnel.
Assists in data management and data analysis
Responsible for the initiation, organization, and carrying out of patient follow-up.
Assesses patient at all follow-up visits.
Attends various meetings pertaining to the clinical trial or research program.
May present information.
May train clinical research staff.
May conduct Quantitative Sensory Pain Testing in the laboratory setting
Performs various duties as needed to successfully fulfill the function of the position.