Night-Shift LVN for Clinical Trials

CenExel

Seal Beach (CA)

On-site

USD 85,962,000 - 94,558,000

Full time

33 hours ago
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Job summary

CenExel Clinical Research is seeking a Licensed Practical Nurse or Licensed Vocational Nurse for a full-time night shift role in California. The position runs 40 hours per week from 11:00 pm to 7:30 am with rotating weekends.

Training lasts two weeks on a morning shift before transitioning to the night schedule. Responsibilities include overseeing daily clinical study activities, assisting with protocol adherence, documenting findings, screening subjects, and coordinating specimen handling under

Qualifications

  • Must hold a current LPN/LVN license in the state where employed.
  • Must be able to communicate clearly with patients.
  • Must have strong interpersonal and teamwork skills.
  • Must be self-motivated and able to work independently.
  • Ability to stay calm and respond to emergencies effectively.

Responsibilities

  • Oversee daily clinical study activities and act as liaison between site and Sponsor.
  • Provide general nursing care: monitor vitals, blood sugar, lab tests, etc.
  • Review and execute clinical research protocols and maintain study documents.
  • Recruit potential study subjects as needed and screen for eligibility.
  • Schedule subjects for assessments and complete Case Report Forms.
  • Maintain inventory of data and supplies and ensure proper laboratory sample handling.
  • Attend training and study meetings; communicate with sponsor and site team.
  • Ensure adverse events are documented and reported; follow CenExel SOPs.

Skills

Nursing skills
Verbal communication
Interpersonal skills
Autonomy
Emergency response

Education

Licensed Practical Nurse or Licensed Vocational Nurse (LPN/LVN)

Job description

CenExel Clinical Research is seeking a Licensed Practical Nurse or Licensed Vocational Nurse for a full-time night shift role in California. The position runs 40 hours per week from 11:00 pm to 7:30 am with rotating weekends.

Training lasts two weeks on a morning shift before transitioning to the night schedule. Responsibilities include overseeing daily clinical study activities, assisting with protocol adherence, documenting findings, screening subjects, and coordinating specimen handling under

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