What are the responsibilities and job description for the Clinical Research Nurse position at Actalent?
LPN/RN or EMT needed at Clinical Research site for overnight shifts! (3 twelve hour shifts per week)
Description
The Study Nurse Coordinator is responsible for coordinating, supervising and monitoring study activities, following adverse events and administering study medications.
Responsibilities
- 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
- 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
Additional Skills & Qualifications:
Must have experience with IVs/injections and be able to provide basic clinical care.
THIS IS AN OVERNIGHT SHIFT; 12 hours with some weekend availability needed
ENGLISH/SPANISH is a MUST for this location
About Actalent:
Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We're supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Description
The Study Nurse Coordinator is responsible for coordinating, supervising and monitoring study activities, following adverse events and administering study medications.
Responsibilities
- 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
- 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
Additional Skills & Qualifications:
Must have experience with IVs/injections and be able to provide basic clinical care.
THIS IS AN OVERNIGHT SHIFT; 12 hours with some weekend availability needed
ENGLISH/SPANISH is a MUST for this location
About Actalent:
Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We're supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
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