Clinical Research RN (Night Shifts)

CenExel; Murray (UT); On-site; USD 50,000 - 58,000; Full time

Benefits offered by this job

Health Insurance

Dental

Vision

LTD

STD

Life Insurance

401k

Job summary

CenExel Clinical Research is seeking a Clinical Research RN I to oversee daily study activities and serve as liaison between the site and sponsor. You will document data accurately and ethically throughout the trial process.

The 3 night shifts per week (6 pm–6 am) include a $3/h night differential and compensation of $36-42/h, based on education, experience, and skill. On-site work with a strong emphasis on quality and regulatory compliance.

Qualifications

• Current RN license in the employing state with no disciplinary action.
• BLS or ACLS certification required or obtainable.
• 1 year or less of clinical experience.
• IV certification required if site demands.
• Capable of performing all licensure-related clinical tasks.
• Strong verbal communication with patients.
• Good interpersonal skills.
• Self-motivated and independent performer.
• Calm under emergencies.
• Professional appearance.
• Oral and written communication skills.

Responsibilities

• Provide nursing care; monitor vitals, lab tests, and related data.
• Review and execute clinical research protocols.
• Complete and maintain study documents per sponsor and site requirements.
• Possibly recruit potential study subjects.
• Screen subjects for eligibility and schedule assessments.
• Complete Case Report Forms per study protocol.
• Coordinate sponsor visits and maintain sponsor communications.
• Maintain inventory of data and supplies.
• Attend training and staff/initiation meetings.
• Observe and report adverse events and serious adverse events.
• Conduct informed consent per CenExel SOPs.
• Follow up on laboratory results and ensure safety.
• Oversee collection/shipment of specimens where applicable.
• Assist with quality assurance activities and complete queries.
• Obtain Principal Investigator signatures on documents.
• Oversee administration of investigational medication per protocol.
• Ensure accountability for study and clinical drugs.
• Adhere to FDA/ICH/GCP and CenExel SOPs.

Skills

Registered Nurse

BLS/ACLS certified

IV certified

Communication skills

Independent worker

Emergency response

Education

RN license in employing state

Job description

About Us

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.

Job Summary

With moderate oversight, the Clinical Research RN I is 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.

Schedule

3 night shifts per week (days vary), 6 pm - 6 am.

Compensation

$36-42/h plus $3/h night shift differential (depending on education, experience, and skillset).

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.
• 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.
• Supports and ensures strictest adherence to best practices, FDA Code of Federal Regulations, ICH (International Conference on Harmonization), GCP (Good Clinical Practices), CenExel standard operating procedures, site working Practices, protocol, and company guidelines and policies.
• 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 the state in which the employee will be working, and not have any disciplinary action on the license.
• Must be BLS or ACLS certified or able to obtain.
• 0-1 year of experience is required.
• Must be IV certified, depending on site.
• 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.
• Must be able to effectively communicate verbally and in writing.

Working Conditions

• Indoor, Clinic 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.
• On-site work arrangement.

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.