About this role
Under direct supervision, responsible for coordinating and participating in clinical research studies conducted by principal investigator, to include recruitment, collection, compilation, documentation and analysis of clinical research data. Assists in the determination of guidelines for the collection of clinical data and/or administration of clinical studies.
- Ability to communicate and liaise with research participants, research team members, and other relevant partner/key stakeholders.
- Demonstrated ability to organize and coordinate work within schedule constraints and handle emergent requirements in a timely manner.
- Demonstrated ability to monitor important and complex projects concurrently.
Education:
Associate’s degree is required.
Experience:
One (1) year nursing experience in the designated study area is required.
Licenses/Certifications:
Active Texas RN license is required.
Active CPR/BLS required.