document scientific research utilizing human subjects. Gathers data and analyzes results. May be responsible for participant recruitment and counseling, ethical oversight, or compilation of study results.
Requisition ID
45306BR
Optional Attachments
Professional License/Certification
Travel Required
Up to 25%
Pay Grade Maximum
145,659.24
Major/Essential Functions
- Develop and maintain relationships with faculty members interested in or currently conducting clinical research.
- Develop and maintain relationships with assigned pharmaceutical, medical device, and other medical manufacturers considering clinical trials.
- Actively market the Clinical Research Institute.
- Facilitate IRB application and submission via Cayuse system.
- Facilitate ongoing and timely communication with the IRB via Cayuse system.
- Recruit and enroll human subject while protecting subjects and subjects’ rights.
- Maintain study files/documents on all assigned studies.
- Facilitates data quality and integrity.
- Assist with development and management of research study budget.
- Assist faculty/staff with development of research protocols.
- Assist with clinical research education and training of volunteers, students, new employees.
- Attend affiliated clinical research meetings and professional meetings where research and compliance training may occur.
- Obtain SoCRA (CCRP) or ACRP (CCRC) certification when eligible.
- Maintain CPR certification.
- Maintain IATA training/certification.
- Maintain required institutional training to be able to participate in Clinical Research activities (i.e. CITI and HIPAA research training).
- Maintain Texas nursing licensure.
- Facilitates data quality and integrity.
- Participate in the Clinical Research call schedule rotation as needed.
- Obtain and maintain appropriate credentialing approval from University Medical Center Medical Staff office.
Grant Funded?
No
Pay Grade Minimum
60,000
Pay Basis
Monthly
Schedule Details
Monday-Friday and occasional weekends and late week nights
Work Location
Lubbock
Preferred Qualifications
- Knowledge of procedures and medications relevant to clinical research trials
- Prior experience working with administrative functions in a clinical setting
- Working knowledge of the following and understanding both treatment and non-treatment protocols.
Department
TTUHSC Clinical Research Institute
Required Attachments
Resume / CV
Job Type
Full Time
Pay Statement
Compensation is commensurate upon the qualifications of the individual selected and budgetary guidelines of the hiring department, as well as the institutional pay plan. For additional information, please reference the institutional pay plan website at https://app4.ttuhsc.edu/payplan/.
Occasional Duties
Occasional on-call schedule. As duties are assigned.
Shift
Day
EEO Statement
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, disability, genetic information or status as a protected veteran.
Required Qualifications
Completion of a Board of Nursing accredited program of professional nursing. Current Registered Nursing license in the state of Texas. Current certification as a Clinical Research Professional or obtains certification upon eligibility or within two (2) years of hire. Obtains and maintains appropriate credentialing approval from affiliated hospitals as required CPR certification, and participation in the call schedule for the Clinical Research Institute. Ability to work with minimal supervision, prioritizing assignments according to the needs of the study or office. Multi-tasking is essential. Able to type.
Does this position work in a research laboratory?
No
