- Facilitates compliances with the research protocol and Good Clinical Practice guidelines.
- uses multiple communication styles and methods to facilitate the effective coordination of clinical trials across disciplines and clinics, acting as a liaison between the principle investigator, sponsoring agent, study patients, referring physicians, pharmacist, statisticians and other members of the research team.
- Takes leadership in ensuring an effective informed-consent process and study subject safety for the duration of the trial.
- Ensures compliance with protocol procedures, assessments and reporting requirements.
- Assists physicians in ensuring adequate source documentation and data-collection that validate the integrity of the clinical trial.
- Assist in enhancing recruitment of study participants, helping with the design and implementation of recruitment strategies for identifying and assessing patients who may be eligible for a clinical trial.
- Demonstrates leadership in adhering to ethical principles in the conduct of clinical trials in order to protect study subjects and data integrity.
- ACRP Certification in Clinical Research Coordination.
- 5 years of experience in Clinical Research. Experience in device, hepatic arterial, and drug based clinical research.
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Clinical Research Nurse II - Louisville, KY, United States - University of Louisville
Description
Department:Location:
Health Sciences Center
Time Type:
Full time
Worker Type:
Regular
Job Req ID:
R104619
Minimum Requirements:
Bachelor's degree in Nursing or a related field, license to practice as an R.N. in Kentucky, and at least 2 years of related experience.
Position Description:
This position's primary role will be to serve as a Clinical Research Nurse II (CRN II). Position is to coordinate clinical research studies conducted at the Department of Surgery, Division of Surgical Oncology patients. Clinical Research at the Department of Surgery, Division of Surgical Oncology includes early phase, novel treatment, multi-centered, cooperative and intergroup trials, multi-institutional device, pharmaceutical trials, hepatic arterial studies, and single- or multi-centered investigator-initiated trials.
Essential Duties and Responsibilities:
Target Compensation Minimum: $65,400
Compensation will be commensurate to candidate experience.
Equal Employment Opportunity
The University of Louisville is an equal opportunity, affirmative action employer, and is committed to providing employment opportunities to all qualified applicants without regard to race, sex, age, color, national origin, ethnicity, creed, religion, disability, genetic information, sexual orientation, gender, gender identity and expression, marital status, pregnancy, or veteran status. If you are unable to use our online application process due to an impairment or disability, please contact the Employment team at or
Assistance and Accommodations
Computers are available for application submission at the Human Resources Department located at 215 Central Avenue, Ste 205 - Louisville, Kentucky 40208.
If you require assistance or accommodation with our online application process, please contact us by email at or by phone
