Research Support Specialist II (S04417P)
Job description
Posting Details
- Assists research personnel in the implementation of research studies to ensure successful completion of study goals.
- Prepares and maintains all Institutional Review Board (IRB) and regulatory paperwork to comply with institutional regulatory requirements.
- Assists in the recruitment and relationship building of study subjects, arranges study visits and provides instructions to meet the goals of the study.
- Collects data from study subjects and enters information into the designated forms/database to comply with study protocols.
- Maintains inventory of supplies or equipment, prepares study kits and requisitions prior to study visits to ensure the appropriate items are available when necessary.
- Builds and maintains a broad network of professional relationships with participants, principal investigator, co‐investigators, research study staff, and other collaborators to ensure successful research collaborations.
- Identifies and reports issues that may affect the accuracy and quality of study design and implementation to meet study aims.
- Performs other duties as assigned.
- Bachelor’s degree with science background.
The following licensure(s), certification(s), registration(s), ect. are required for this position, which must be maintained in good standing:
- Citi course in the protection of human research subjections certification through collaborative institutional training initiative (Citi) within 90 days of hire.
- Research experience working with human participants and related methodological techniques.
- Experience working with Institutional Review Board applications, coordinating regulatory files/ study binders, and ensuring adherence to good clinical practice.
Preferred/Optional licensure(s), certification(s), registration(s), ect. are required for this position, which must be maintained in good standing and must be obtained within six moths of qualification:
- Clinical Research coordinator certification through association of Clinical Research Professionals (ACRP) or
- Certified Clinical Research Professional Certification through Society of Clinical Research Associates (SOCRA).
- Basic Life Support Certification.
UTA is an Equal Opportunity/Affirmative Action institution. Minorities, women, veterans and persons with disabilities are encouraged to apply. Additionally, the University prohibits discrimination in employment on the basis of sexual orientation. A criminal background check will be conducted on finalists. The UTA is a tobacco free campus.
Requirement Questions
Required fields are indicated with an asterisk (*).
- * What is the highest degree you have attained? (Please specify in your resume)
- Associate's degree
- Bachelor's degree
- Master's degree or higher
- None of the above
- * What is your skill level using Microsoft Office Suite (Word, Excel, PowerPoint, Outlook, etc)? (Proficient is the highest skill level)
- No skills/Basic
- Intermediate
- Advanced
- Proficient
- * How many years of experience do you have working in research?
- None/less than 1 year
- 1 to 2 years
- 3 to 4 years
- 5 years or more
Documents Needed To Apply
- Resume or CV
- Cover/Interest Letter
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