Coord,Research
About The Position
The Division of Nephrology, within the Department of Internal Medicine, is seeking a full-time candidate who is a detail-oriented, results driven individual to join our team as a Clinical Research Coordinator. In general, the ideal candidate for the Nephrology Research Coordinator position will have experience coordinating clinical trials with all populations, including Hispanic and/or Native American communities. This includes completing IRB submissions (local and external), patient recruitment and retention, and data collection and maintenance. This candidate will also have a firm understanding of good clinical practices in conducting research strong interpersonal and communication skill and the ability to work effectively with a variety of university and community stakeholders. Depending on the study, these stakeholders might include: health care providers, funding agencies, university researchers, and media representatives. The ideal candidate will exhibit the following characteristics: Ability to effectively adapt to changing priorities Ability to effectively provide support for a variety of research project types Ability to effectively multitask Ability to communicate effectively, both orally and in writing Ability to communicate effectively in Spanish both orally and in writing Specific duties will include: Recruitment, enrollment, and scheduling of research subjects. Developing and maintaining record keeping systems and procedures Collecting and preparing comprehensive statistical and narrative program reports, such as enrollment tracking for all active studies Coordinates and facilitates development and submission of local IRB applications for the conduct of biomedical and/or other federally regulated life sciences research studies, in accordance with all relevant Federal and State regulations and guidelines Advise and assist research in the preparation and submission of protocols for compliance review Drawing and processing blood will be required for some studies See the Position Description for additional information.
Requirements
- Bachelor's degree; at least 1 year of experience directly related to the duties and responsibilities specified.
- Completed degree(s) from an accredited institution that are above the minimum education requirement may be substituted for experience on a year for year basis.
Nice To Haves
- Recruiting patients to participate in research studies
- Preparing applications and other documents for submission to an Institutional Review Board (IRB) or direct experience in IRB Administration
- Coordinating clinical trials
- Drawing and processing blood (experience and/or training)
- Ability to work flexible hours, as required by study
- Use and understanding of medical terminology
- Fluent in Spanish (speaking, reading, and writing)
- Ability to travel, as required by study
Responsibilities
- Recruitment, enrollment, and scheduling of research subjects.
- Developing and maintaining record keeping systems and procedures
- Collecting and preparing comprehensive statistical and narrative program reports, such as enrollment tracking for all active studies
- Coordinates and facilitates development and submission of local IRB applications for the conduct of biomedical and/or other federally regulated life sciences research studies, in accordance with all relevant Federal and State regulations and guidelines
- Advise and assist research in the preparation and submission of protocols for compliance review
- Drawing and processing blood will be required for some studies
Benefits
- medical, dental, vision, and life insurance
- educational benefits through the tuition remission and dependent education programs
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
