WCCT is a multisite, full-service pharmaceutical contract research organization (CRO) of outsourced early drug development and late phase CRO services to the pharmaceutical, biotechnology and medical device industries. We are the specialized global drug development professionals who offer an innovative, agile and collaborative approach to every program we deliver.

JOB SUMMARY

The clinical research nurse is required to have an in-depth knowledge of protocol requirements and good clinical practices as set forth by regulations. The clinical research nurse will provide patient care, perform ongoing assessments, and document in accordance with standards and regulatory guidelines pertaining to specified research patients enrolled onto clinical trials, when needed by the research team.

ESSENTIAL JOB FUNCTIONS

Responsible for following all study and non-study regulations including but not limited to: HIPAA, OSHA, and GCP/GDP; as well as proper safety and emergency policies and procedures as set forth by WCCT

Complete study procedures, including but not limited to vital signs, electrocardiogram, blood collection, meal distribution, pulmonary function tests, check in/out of volunteers, urine/stool sample collection, CSF collection, IV insertions and med administration (including IM, SW, rectal, oral, and IV fluid administration)

Perform all forms of dose administration, as allowed per licensure, included but not limited to: IV, IM, SQ and oral, etc.

Perform nursing assessments and monitor subjects' progress during clinical studies and notify PI/CRC/CN of any adverse events and serious adverse events, including evidence of unexpected side effects. Perform interviews, as needed, during each subject visit and follows procedures as specified per protocol.

Enter subject information into subject source/facility database, and QC entries, as needed.

May cross-train to cover Charge Nurse in case coverage is needed; must be able to do the following when covering:

Consistently monitor and manage the conduct all protocols, staff, and subject population within the Clinical Support Department

Ensure safety and compliance of floor

Develop and serve as a resource to ensure staff’s skills are maintained and enhanced

Be able to provide medical care, both emergent and non-emergent, to all subjects and floor staff if needed

Assist Clinical Research Coordinators with study responsibilities and necessities

Duties on the floor: Atomic Clock synchronization, Maintain work area cleanliness of unit, Assist in head count of subjects in-house, Assist in the Quality Control of: tubes, source/PK logs, procedures, Assist with preparation of ALL study set-ups, Assist with the maintenance of supplies and equipment for all study relate procedures, Prepare for and assist with admission procedures, Assist with room assignments for studies

EDUCATION, EXPERIENCE, CERTIFICATES, LICENSES AND TRAINING

Education

High school diploma or General Education Degree (GED), 3-6 months related experience and/or training, or the equivalent combination of education and experience is required.

Associate’s degree or higher in Nursing

Experience/Training

Study-related training prior to performing study-related procedures

Module 1, 2, 3, 6, 7 training required

Ability to read and interpret documents such as Standard Operating Procedures (SOP), safety rules, study-related forms and documents. Ability to write routine reports and accurately record information on forms and/or documents. Ability to effectively communicate with subjects, employees, supervisors, and others on study-related matters in English is necessary

Certificates & Licenses

Current BLS/ACLS certification is required

Current PALS certification is preferred

Licensed Vocational Nurse (LVN) license is required

All your information will be kept confidential according to EEO guidelines.