Licensed Vocational Nurse - Clinical Research (6:00 pm - 6:00 am)

CenExel•Riverside, CA

About The Position

CenExel Clinical Research is hiring a Licensed Vocational Nurse to oversee daily clinical study activities and serve as a liaison between the investigative site and the Sponsor. The role requires accurate and ethical documentation throughout the clinical research process and providing general nursing care to study participants as needed. The schedule is three 12-hour shifts, from 6:00 pm to 6:00 am, with weekend availability as part of the normal schedule. Paid training lasts two weeks and takes place on a morning shift; afterward, the employee will work the regular overnight shift. The stated hourly range is $29.00–$30.00, depending on education, experience, and skillset, plus four hours of overtime each day. The position is based in an indoor office environment. Essential physical activities include sitting, typing, standing, and walking; the role 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.
Communicate clearly verbally with patients.
Have 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.
Reflect the company’s professional image and uphold its vision through actions and demeanor.
Be available to work three 12-hour overnight shifts, 6:00 pm to 6:00 am, including weekends as part of the normal schedule.
Attend two weeks of paid morning-shift training before starting the normal overnight schedule.
Occasionally lift up to 20 pounds and perform sitting, typing, standing, and walking.
Report to work as scheduled.

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.
Possibly recruit potential study subjects.
Screen subjects for eligibility and schedule study-specific assessments as designated on the Delegation of Authority Log.
Complete and maintain Case Report Forms consistent with source documentation and study protocols.
Accompany sponsor representatives during visits and maintain effective, 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, when applicable.
Answer questions from support staff, study patients, or 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.