Highlights
- $80,000 - $95,000 salary
- Great benefits including 20 days of PTO and 401k with a match!
- Consistent M-F schedule, no weekends or nights
- Focus on studies in Alzheimers, Parkinson's, MS, and more!
The Company
Our client is a unique clinical site network that focuses on studies in Alzheimer's, Dementias, and Parkinson's disease. They pride themselves on developing strong relationships with clinical sites to bolster up their resources, quality, and patient care in these key therapeutic areas.
The Role:
Play an integral role for leading the coordination and management of assigned Clinical Research protocols. This includes screening potential patients for eligibility, providing study specific education to patients, conducting informed consent discussions and visits, and acting as a liaison with internal and external stakeholders involved in the clinical trial activities. This position interacts with a variety of people, both internal and external!
- Provide nursing expertise to the research team during study development and implementation
- Facilitate education of the team on study requirements.
- Identify and assist with procuring equipment and supplies for the trial requirements
- Facilitate the initial and ongoing informed consent/assent process with research participants
- Ensure the trial is conducted according to the protocol, ICH/GCP and FDA guidelines.
- Collect specimens (blood, urine, CSF, tumor samples) for clinical and research testing
- Facilitate the processing and shipment of research specimens
- Obtain medical histories and conduct safety assessments such as vital signs, EKGs and report potential adverse events
- Record research data in approved source documents and into study-specific databases.
- Prepare for and participate in site monitoring visits and/or audits
- Assist in the development of Standard Operating Procedures and Work Instructions
Qualifications
- RN degree
- 1+ years of experience in Clinical Research
- Ability to work on site in Tampa