Surgical Clinical Research RN; Night Shift

Surgical Clinical Research RN (Night Shift)

Join to apply for the Surgical Clinical Research RN (Night Shift) role at Cen Exel

Each of Cen Exel’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 inpatient capability.

We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.

Thursday, Friday, Saturday 6 pm - 6 am.

• 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 Cen Exel 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