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

CenExel•Anaheim, CA

26d•$39 - $42•Onsite

About The Position

The Registered Nurse - Clinical Research oversees the implementation of daily clinical study activities, serves as a liaison between the investigative site and the Sponsor, and accurately and ethically documents information obtained throughout the clinical research process. The role provides nursing care to study participants, supports study procedures and medication administration, and follows participants throughout their study stay in accordance with protocol. CenExel sites conduct Phase I to Phase IV clinical trials across specialties including Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. The position is based in an indoor office environment. The posted schedule information includes 11:00 pm–7:30 am, availability to work weekends, and a 2–3 week training period requiring availability for an AM shift. Reporting to work as scheduled is essential. The job posting also lists an hourly range of $39.00–$42.00, with an additional $3.00 per hour differential after 90 days, depending on education, experience, and skillset.

Requirements

Current Registered Nurse license in California.
Capability to perform clinical tasks relevant to licensure and/or training.
Ability to communicate clearly verbally with patients.
Good interpersonal skills in interactions with patients, staff, and sponsor representatives.
Self-motivation and ability to perform tasks independently.
Ability to react calmly and effectively in emergency situations.
Professional conduct that reflects the company’s image and upholds its vision.
Availability to work the stated schedule and weekends.
Availability to work an AM shift during a 2–3 week training period.

Responsibilities

Provide general nursing care to study participants, including monitoring vital signs and blood sugar and performing or assisting with 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 consistent 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 informed consent in accordance with 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 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 assigned duties and responsibilities.