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Paramedic
Fortrea
Daytona Beach, USA
Full-time
Entry · 2+ years experience
Onsite
Discovered 2 days ago
ECGGood Clinical Practice (GCP)Standing Ordersstandard operating procedures (SOPs)
Free
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ECGGood Clinical Practice (GCP)Standing Orders
Key Skills for This Role
ECGGood Clinical Practice (GCP)Standing Ordersstandard operating procedures (SOPs)
Full Job Posting
WHAT YOU WILL DO
- Under the direction and medical oversight of the Physician/Investigator, the Paramedic acts as a primary safety contact for study participants within a Fortrea Clinical Research Unit (CRU). The paramedic monitors the study participants within the Fortrea CRU at all times, ensuring their continuous safety and well-being.
Other key responsibilities
- Collaborate clearly and effectively with physicians, nurses, and other medical team members to support coordinated participant care.
- Deliver basic and advanced medical care, within their defined scope of practice, to study participants in both emergent and non-emergent situations, as appropriate.
- Lead resuscitation and stabilization efforts for participants experiencing life-threatening situations, following accepted medical protocols and any study-specific treatment requirements.
- Monitor, document, and review active Adverse Events (AEs); communicate significant findings to the investigator and support ongoing safety assessments. Escalate any participant safety concerns to the investigator for review and determination regarding study procedures and/or dosing.
- Review active AEs for assigned studies and follow up with study participants as needed.
- Administer medications and treatments as prescribed by the investigator or physician and in accordance with study protocols, Standing Orders, and site procedures.
- Perform technical procedures as needed, including blood collection, vital sign measurement, ECGs and other delegated clinical activities in accordance with protocol requirements, SOPs, and applicable regulations.
- Assess participants with out-of-range values for associated signs or symptoms, initiate appropriate interventions within scope of practice, and promptly notify the investigator when clinically indicated.
- Conduct all study-related activities in accordance with study protocols, Investigator instructions, Standing Orders, applicable regulations, Good Clinical Practice (GCP), and Fortrea policies and standard operating procedures (SOPs).
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