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

CenExel

Los Alamitos (CA)

On-site

USD 55,000 - 59,000

Full time

4 days ago
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Benefits offered by this job

Health Insurance
Dental
Vision
LTD
STD
Life Insurance
401k

Job summary

CenExel Clinical Research is seeking a Registered Nurse (CA) to oversee daily clinical study activities at our CA site. You will act as a liaison between the site and Sponsor, perform essential nursing tasks, and ensure protocol adherence and accurate documentation throughout the study.

Ideal candidates are licensed in California, capable of handling emergencies calmly, and able to work independently while maintaining professional standards and effective communication with patients, staff, and

Qualifications

  • 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.

Responsibilities

  • Oversee daily clinical study activities and liaise between site and Sponsor.
  • Provide general nursing care, monitor vitals, labs, and reports as required.
  • Review and execute clinical research protocols and maintain study documents.
  • Screen subjects for eligibility and schedule assessments.
  • Maintain study logs and ensure proper collection and shipment of specimens where applicable.
  • Attend training and meetings and respond to investigator questions as needed.
  • Ensure accountability for investigational medications and adherence to protocols.

Skills

RN CA license
Clinical tasks competency
Verbal communication
Interpersonal skills
Independent work
Emergency response
Professional demeanor

Education

Registered Nurse, CA

Job 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

$40.00 – $43.00 (Depending on education, experience, and skillset)

Schedule: Monday - Friday 03:00 pm - 11:30 pm + rotating 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
  • Indoor, Office environment.
  • Essential physical requirements include sitting, typing, standing, and walking.
  • Lightly active position, occasional lifting of up to 20 pounds.
  • 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

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