Celerion

Global CRO for early-phase development

Bilingual Registered Nurse

Nursing & Frontline Patient CareConfirmed live in the last 24 hours

Full-timeTempe, AZ, USANo salary listedIn-person

About the Job

Requirements

Registered Nurse (RN) licensed in the practicing state.
One year of clinical practice experience with assessment skills.
Current CPR certification.
Ability to respond to study participant needs, including lifting, bending, and crouching.
Exposure to human biological samples.
Strong assessment, reasoning, and medical/nursing assessment skills.
English-Spanish spoken fluency is required and tested.
Ability to work a flexible schedule up to 40 hours, Monday through Friday, with possible weekends.

Responsibilities

Perform nursing tasks, including taking vital signs, performing electrocardiograms (ECGs), and drawing blood.
Train clinical associates on electrocardiogram procedures, manual vital procedures, and assessment skills related to reporting adverse events.
Perform other clinical procedures necessary for study conduct.
Perform, monitor, and/or train invasive and non-invasive dosing procedures.
Assess, identify, and report adverse events to medical staff, including the safety nurse, medical director, and physician.
Implement and execute emergency procedures.
May administer informed consent forms.

Desired Qualifications

Emergency Medical Technician/Paramedic (EMT-P) or Respiratory Technician qualification with advanced cardiac life support, or other emergency experience.
Emergency or intensive care medical experience.

Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.

Celerion is seeking a Full-time Nurse to assist with our clinical research trials. This is a dynamic role working with a healthy population, offering the ability to learn about clinical research and see the drug development process at work.

Essential Functions

Qualified to perform all nursing tasks (vital signs, ECGs, draw blood, etc)

Train clinical associates on Electrocardiogram (ECG) procedures, manual vital procedures and assessment skills related to reporting Adverse Events (A/E's)

Perform other clinical procedures necessary for study conduct

Certified to perform, monitor, and/or train invasive and non-invasive dosing procedures

Assess and identify and report adverse events to medical staff (safety nurse, medical director, physician)

Able to implement and execute emergency procedures

May administer Informed Consent Forms

Qualifications

RN (licensed in practicing state)

1 year of clinical practice experience with assessment skills

Emergency Medical Technician/Paramedic (EMT-P) or Respiratory Technician with Advanced cardiac life support or other emergency experience desirable

Emergency or Intensive Care medical experience preferred

Current CPR certification

Ability to respond to study participant needs (i.e. lifting, bending, crouching, etc.)

Exposure to human biological samples

Strong assessment skills

Strong reasoning skills

Strong medical/nursing assessment skills

Detail oriented

Professional and positive attitude

Flexible work schedule up to 40 hours (Mon-Friday and possible weekends)

English-Spanish bilingual spoken fluency is required and tested.

Celerion Values: Integrity Trust Teamwork Respect

Are you ready to join our team?

Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.

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About the Company

Celerion

Global CRO for early-phase development

Celerion is a global contract research organization focused on early-phase drug development. It conducts contracted research across clinical trial design, feasibility studies, project management, clinical and medical monitoring, bioanalytical sciences, and regulatory affairs, using High Resolution Mass Spectrometry-based metabolite profiling to inform decisions. Its advantage comes from over 40 years of experience, specialized metabolite profiling, and a global, integrated service model that accelerates development timelines. The goal is to help pharmaceutical and biotech clients bring safe and effective treatments to patients faster through rigorous, high-quality research.

Company size: 1,001-5,000
Company stage: Acquired
Total funding: Not listed
Headquarters: Lincoln, NE
Founded: 2010

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