Dosing Nurse

Posted 16 Days Ago
Be an Early Applicant
56529, Dilworth, MN, USA
In-Office
30-36 Hourly
Entry level
Pharmaceutical
The Role
Administers or assists with dosing study subjects during clinical research trials, following study protocols and healthcare practices. Ensures proper study-product administration, communicates clearly with staff and subjects, and accurately documents dosing activities, training, and licensure. Performs additional assigned duties while maintaining compliance with applicable procedures.
Summary Generated by Built In

The primary purpose of a Dosing Nurse is to dose or assist with dosing subjects during clinical research trials.  They will ensure that any dosing activities completed are per protocol and follow acceptable healthcare practices.

Essential Functions

  • Ensure proper procedure is utilized in the method needed to administer study product.
  • Communicate effectively with staff and subjects to ensure clarity of duties.
  • Provide accurate and completed documentation of activities, training and licensure.
  • Execute other duties as assigned
Qualifications

Knowledge, Skills and Abilities

Communication

 

Professionalism

Education Requirements

Required: Certificate or degree necessary for licensure.

Certification Requirements (If Applicable)

Required: Current MN LPN or RN license.

Skills Required

  • Certificate or degree necessary for licensure
  • Current Minnesota LPN or RN license
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The Company
HQ: Hyderabad
563 Employees
Year Founded: 2004

What We Do

AXIS Clinicals Limited is one of the most experienced and fastest growing Clinical Research Organization. Our state-of-the-art facilities houses 500+ dedicated full-time professionals to ensure the quick turn around time with high quality. Our facilities are accredited by DCGI (Drugs Controller General – India), NABL (National Accreditation Board for Testing and Calibration Laboratories - ISO 15189:2003) and inspected by US-FDA, UK-MHRA, Brazil-ANVISA, France –AFSSAPS / ANSM, GCC, MCC-South Africa etc. Within short span, we have achieved the milestone of completing 2750+ clinical studies and 1000+ product approvals from various regulatory agencies. 65+ regulatory audits from global competent authorities is testament to our professionalism and dedication to quality studies. Our Phase II – IV capabilities are growing along with an extended portfolio of Site Management, Medical Writing, and Data Management.

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