Registered Nurse - Clinical Research (03:00 pm - 11:30 pm)

CenExel•Anaheim, CA

25d•Onsite

About The Position

CenExel Clinical Research is hiring a Registered Nurse to oversee daily clinical study activities and serve as a liaison between the investigative site and study sponsors. The nurse provides participant care, ensures study procedures and documentation comply with protocols and site and sponsor requirements, and supports participant safety throughout clinical research studies. The schedule information in the posting is inconsistent: the title lists 03:00 pm–11:30 pm, while the schedule section lists 11:00 pm–7:30 am. The role also requires weekend availability and availability for an AM shift during a 2–3 week training period. The position is in an indoor office environment and involves sitting, typing, standing, and walking, with occasional lifting of up to 20 pounds. The hourly range is $39.00–$42.00, depending on education, experience, and skillset, with an additional $3.00 per hour differential after 90 days. Full-time employees are eligible for the stated benefits after 30 days of employment.

Requirements

Current Registered Nurse license in California.
Ability to perform clinical tasks relevant to licensure and/or training.
Ability to communicate clearly with patients verbally.
Good interpersonal skills in interactions with patients, staff, and sponsor representatives.
Self-motivated and able to perform tasks independently.
Ability to react calmly and effectively in emergency situations.
Professional conduct that reflects the company’s image and vision.
Must be available to work weekends.
Must be available to work an AM shift during a 2–3 week training period.
Ability to perform the essential physical activities of sitting, typing, standing, and walking, and occasional lifting of up to 20 pounds.
Ability to report to work as scheduled.

Responsibilities

Provide general nursing care to study participants, including monitoring vital signs and blood sugar and conducting lab tests.
Review and execute clinical research protocols.
Complete and maintain study documents in accordance with sponsor and site requirements.
Recruit potential study subjects when applicable.
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 effective ongoing communication with sponsors.
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.
Be on call to answer questions from support staff, study patients, or other medical staff as necessary.
Assist with quality assurance activities and complete queries as applicable.
Obtain Principal Investigator signatures on necessary documents.
Oversee or coordinate investigational medication administration 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.