Clinical Trials Nurse- Full Time

CenExel is a leading nationwide clinical research site and patient network serving the life sciences industry. Leading in CNS and early phase studies, our 18 science-led Centers of Excellence deliver the right patients, at the right time, in the right place. Recently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials. Our world-class PIs, advanced patient engagement strategies, premium data analytics, and integrated operations optimize every step of the clinical trial process.

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.

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.

Shift : 6 am - 6 pm, days vary based on study schedule.

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.

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.

Follows up appropriately on all laboratory results.

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.

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.

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 IV certified, depending on site.

Must be capable of performing all clinical tasks relevant to licensure and/or training.

Ability to react calmly and effectively in emergency situations.

Must be able to effectively communicate verbally and in writing.

Indoor, Clinic environment.

Essential physical requirements include sitting, typing, standing, and walking.

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.