LVN (Friday, Saturday, Sunday) - Clinical Research

CenExel•Los Alamitos, CA

About The Position

The LVN oversees the implementation of daily clinical study activities and serves as a liaison between the investigative site and the Sponsor. The role requires accurate and ethical documentation throughout the clinical research process and provides general nursing care to study participants, including monitoring vital signs, blood sugar, and laboratory tests. The position is part-time, 24 hours per week, scheduled Friday through Sunday from 3:00 p.m. to 11:30 p.m. Training lasts two weeks on a morning shift, after which the regular schedule begins. The hourly range is $32.00–$34.00, depending on education, experience, and skillset. The work takes place in an indoor office environment. Essential physical activities include sitting, typing, standing, and walking; the position is lightly active and may occasionally require lifting up to 20 pounds. Reporting to work as scheduled is essential.

Requirements

Hold a current Licensed Practical Nurse or Licensed Vocational Nurse license in the state where the employee will work.
Be capable of performing clinical tasks relevant to licensure and/or training.
Clearly communicate verbally with patients.
Demonstrate good interpersonal skills in interactions with patients, staff, and Sponsor representatives.
Be self-motivated and able to perform tasks independently.
React calmly and effectively in emergency situations.
Maintain the professional image of the company and uphold its vision through actions and demeanor.

Responsibilities

Provide general nursing care to study participants, including monitoring vital signs, blood sugar, and laboratory tests.
Review and execute clinical research protocols.
Complete and maintain study documents in accordance with sponsor and site requirements.
Recruit potential study subjects as needed.
Screen subjects for eligibility and schedule study-specific assessments as designated on the Delegation of Authority Log.
Complete and maintain Case Report Forms in agreement with source documentation and study protocols.
Accompany Sponsor representatives during visits and maintain ongoing communication with the Sponsor.
Maintain adequate inventory of data and supplies.
Attend training, staff, initiation, study start-up, and other assigned meetings.
Observe, document, report, and follow up on adverse events and serious adverse events.
Conduct the informed consent process according to CenExel Standard Operating Procedures.
Follow up appropriately on laboratory results.
Maintain safety standards while performing job responsibilities.
Maintain study logs and site relations.
Ensure proper collection, processing, and shipment of laboratory specimens, if applicable.
Answer questions from support staff, study patients, or other medical staff while on call, as necessary.
Assist with quality assurance activities and complete queries, as applicable.
Obtain Principal Investigator signatures on necessary documents.
Oversee or coordinate administration of investigational medication and follow subjects throughout their study stay according to protocol.
Ensure accountability and adequate supply of study and clinical drugs.
Perform other duties and responsibilities as assigned.