Licensed Vocational Nurse - Clinical Research (Friday, Saturday, Sunday)

About the role

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 include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each Center of Excellence has extensive 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.

Working Shift

Part-Time 24 hours a week - 3:00 pm - 11:30 pm (Friday, Saturday and Sunday)

Paid training

Paid training is for 2 weeks, working a morning shift. Once training is completed, you will be scheduled for your normal shift going forward.

Hourly Range

$32.00 - $34.00/hour (Depending on education, experience, and skillset)

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.
• Serves as a liaison between the investigative site and the Sponsor.
• Accompanies sponsor representatives during their visits and maintains effective and ongoing communication with the sponsor.
• Maintains adequate inventory of all data and supplies.
• Completes and maintains Case Report Forms in agreement with the source documentation and in accordance with study protocol.
• Screens subjects for eligibility, and schedules subjects for study specific assessments, as designated on the Delegation of Authority Log.
• 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.

Education/Experience/Skills

• Must be a Licensed Practical Nurse or Licensed Vocational Nurse with a current license in the state in which the employee will be working.
• 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.

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.