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

Anaheim Clinical Trials, LLC; Anaheim (CA); On-site; USD 81,000 - 87,000; Full time

Benefits offered by this job

Health Insurance

Dental

Vision

LTD

STD

Life Ins

401k

Job summary

CenExel Clinical Research in Anaheim, CA is seeking a Registered Nurse for clinical trials on the 3:00 pm - 11:30 pm shift. You will oversee daily study activities, monitor participants, and document findings, serving as liaison between the site and Sponsor.

The role requires a CA RN license, ability to perform licensure-relevant tasks, and strong communication. Training includes an initial AM shift; weekends required.

Qualifications

• Must be a Registered Nurse with a CA license.
• Ability to perform clinical tasks relevant to licensure.
• Clear verbal communication with patients and staff.
• Strong interpersonal skills and independence.
• Calm under pressure and professional in demeanor.

Responsibilities

• Provide general nursing care, monitor vitals and lab results.
• Review and execute clinical research protocols.
• Document study data accurately and ethically.
• Recruit and screen potential study subjects when needed.
• Coordinate with sponsor and maintain study logs.

Skills

Registered Nurse

Clinical research

Communication

Emergency response

Education

CA RN license

Job description

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

Job Category: Clinical Research Staff

Requisition Number: REGIS004394

• Posted : October 14, 2026
• Full-Time
• On-site

Locations

Showing 1 location

• Travel Required : No

Description

Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.

Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full-time employees after 30 days of employment, including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.

HOURLY RANGE

$39.00 - $42.00 + $3.00/hour differential pay after 90 days of employment ( Depending on education, experience, and skillset )

Schedule: 11:00 pm - 7:30 am + must be available to work weekends

Training period of 2-3 weeks will require being available to work an AM shift.

Responsible for overseeing the implementation of daily clinical study activities. Serving as a liaison between the investigative site and the Sponsor. Responsible for accurately and ethically documenting all information obtained throughout the clinical research process.

Essential Responsibilities and Duties:

• Provides general nursing care to study participants as necessary; including, but not limited to monitoring of vitals, blood sugar, vital signs, lab tests, etc.
• Reviews and executes clinical research protocols.
• Completes and maintains study documents in accordance with sponsor and site requirements.
• Possible recruitment of potential study subjects.
• Screens subjects for eligibility, and schedules subjects for study specific assessments, as designated on the Delegation of Authority Log.
• Completes and maintains Case Report Forms in agreement with the source documentation and in accordance with study protocol.
• Accompanies sponsor representatives during their visits and maintains effective and ongoing communication with the sponsor.
• Maintains adequate inventory of all data and supplies.
• Regularly attends training meetings, staff meetings, initiation meetings, study start-up meetings, and other meetings as assigned.
• Observes, documents, reports, and follows up on adverse events and serious adverse events.
• Conducts the informed consent process, per CenExel Standard Operating Procedures.
• Follows up appropriately on all laboratory results.
• Maintains safety standards when performing job responsibilities.
• Maintains study logs and site relations
• Ensures proper collection, processing, and shipment (if applicable) of laboratory specimens.
• Is on call to answer questions for other members of support staff, study patients or other medical staff, as necessary.
• Assists with quality assurance activities and completes queries, as applicable.
• Obtains Principal Investigator signatures on necessary documents.
• Oversees or coordinates the administration of investigational medication and follows
• subjects throughout the study stay, per protocol.
• Ensures accountability and adequate supply for study and clinical drugs.
• Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.

Education/Experience/Skills:

• Must be a Registered Nurse with a current license in CA
• Must be capable of performing all clinical tasks relevant to licensure and/or training.
• Must be able to clearly communicate verbally with patients.
• Must have good interpersonal skills, demonstrated through interactions with patients, staff, Sponsor representatives, etc.
• Must be self-motivated and able to perform tasks independently.
• Ability to react calmly and effectively in emergency situations.
• Must reflect the professional image of the company, upholding the company vision in actions and demeanor.

Working Conditions:

1. Indoor, Office environment.
2. Essential physical requirements include sitting, typing, standing, and walking.
3. Lightly active position, occasional lifting of up to 20 pounds.
4. Reporting to work, as scheduled, is essential.

CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status

Travel Required

No .

Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.For further information, please review the Know Your Rights notice from the Department of Labor.