Clinical Research facility in Miami is looking for Study Nurse/Clinical Research nurses for variety of shift
The Study Nurse Coordinator is responsible for coordinating, supervising and monitoring study activities, following adverse events and administering study medications.
To ensure study data is collected to a high quality in accordance with Good Clinical Practice (GCP) standards.
To ensure subject safety at all times
Other tasks and responsibilities will include:
-Responsible for administering study medication to study participants.
-Familiar with intravenous infusion techniques including pumps.
-Responsible for supervising staff and study events on the unit according to protocol requirements.
-Responsible for making staff adjustments during absences or others unanticipated work circumstances.
-Responsible for monitoring study schedules and reviewing study activities as they progress.
-Responsible for reviewing, recording and following adverse events.
-Responsible for confirming that a complete screening chart containing informed consents, lab results and Investigator approval is available on the day of admission for every admitted subject.
-Responsible for monitoring clinical results, compliance, and/or safety issues which would trigger the exclusion or discontinuation of a participant.
-Ability to effectively interact with pharmaceutical company representatives (monitors) and clinical research organizations (CRO) in response to queries during the course of the research study.
-Participates in protocol meetings with pharmaceutical company representatives.
-Assures that all necessary source documents are available on the unit on a timely basis.
-Reviews study source documents for completion.
-Assists with new employee (regular and per diem) training by providing orientation to general study procedures and responsibilities.
data management, clinical trial, Registered Nurse, Med Surg, bilingual, clinical research
Additional Skills & Qualifications:
LPN or BSN or RN with at least 2 years of experience preferably in a clinical research environment or patient care setting
Fluent in English/Spanish preferred but not required
Strong computer skills and the ability to document study finding, and adverse events or Case management.
Must have previous exp doing or injecting
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