HomeFloridaStudy Nurse Coordinator

Miami, FL

Study Nurse Coordinator

Location7501 SW 117th Ave, Miami, Florida 33186
Employment TypeContractor
Date Posted2022-08-07
Direct Apply
Valid Through2023-04-10

Job Description:

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.

Clinical Operations/Medical/Screening

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

Experience Level:

Intermediate Level

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.

Job ID: 2124388473497522298

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