Clinical Research Coordinator -
Job Number:
240611
Organization
: Anesthesiology
Job Location
: Oklahoma-Oklahoma City-Health Sciences Center
Schedule
: Full-time
Work Schedule: M-F
Work Type: Onsite
Salary Range: Targeted salary up to $50,400 annually, based on experience
Benefits Provided: Yes
Required Attachments: Curriculum Vitae
Job Description
---
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.
Duties:
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.
Performs various duties as needed to successfully fulfill the function of the position.
Job Requirements
---
Education: Bachelor's Degree
- 12 months of clinical practice, nursing, or clinical trial or research program coordination experience
Equivalency/Substitution: Will accept 48 months of equivalent experience in lieu of a Bachelor's Degree for a total of 60 months experience or a Master's Degree in lieu of experience
Certifications/Licenses:
Oklahoma State licensure is required for Nurses and Physician Assistants
Basic Life Support (BLS) or able to obtain within 30-days from hire date
Skills:
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
Preferred:
- 24 months of clinical practice, nursing, or clinical trial or research program coordination experience
Working Conditions:
- Physical: Sitting for prolonged periods, manual dexterity, speaking and listening, reaching, bending, standing and stooping.
- Environmental: Clinic environment, exposure to infectious diseases.
Equal Employment Opportunity Statement: The University of Oklahoma, in compliance with all applicable federal and state laws and regulations, does not discriminate on the basis of race, color, national origin, sex, sexual orientation, genetic information, gender identity, gender expression, age, religion, disability, political beliefs, or status as a veteran in any of its policies, practices, or procedures. This includes, but is not limited to, admissions, employment, financial aid, housing, services in educational programs or activities, and health care services that the University operates or provides.
Why You Belong at the University of Oklahoma: The University of Oklahoma fosters an inclusive culture of respect and civility, belonging, and access, which are essential to our collective pursuit of excellence and our determination to change lives. The unique talents, perspectives, and experiences of our community enrich the learning, and working environment at OU, inspiring us to harness our innovation, creativity, and collaboration for the advancement of people everywhere.
Hiring contingent upon a Background Check?: Yes
Special Indications: None
Job Posting
: Mar 6, 2024
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