Clinical Research RN

Providence•Lacey, WA

3d•Onsite

About The Position

This position handles the clinical responsibilities of the clinic trial. Acts as a liaison between the investigative site and the sponsor and retrieves data and records before a monitors visit. The research coordinator is the study sites organizer of day-to-day conduct of study activities, including completing case report forms, maintaining study files, maintaining drug accountability and integrity, and assisting the investigator and sub investigators as needed. They are responsible for assessing patient toxicity and patient education regarding treatment plan medications, informed consent, adverse events and disease process and protocol requirements. Providence caregivers are not simply valued – they’re invaluable. Join our team at Providence Centralia Hospital and thrive in our culture of patient-focused, whole-person care built on understanding, commitment, and mutual respect. Your voice matters here, because we Providence know that to inspire and retain the best people, we must empower them.

Requirements

Graduate of an accredited Registered Nurse Program.
Washington Registered Nurse License (Upon hire).
National Provider BLS - American Heart Association (Upon hire).
2 years Acute care or oncology nursing experience.

Nice To Haves

Certified Clinical Research Coordinator (Upon hire).
2 years Experience in clinical research or familiarity with clinical trials.

Responsibilities

Handles the clinical responsibilities of the clinic trial.
Acts as a liaison between the investigative site and the sponsor.
Retrieves data and records before a monitors visit.
Organizes day-to-day conduct of study activities.
Completes case report forms.
Maintains study files.
Maintains drug accountability and integrity.
Assists the investigator and sub investigators as needed.
Assesses patient toxicity.
Provides patient education regarding treatment plan medications, informed consent, adverse events, disease process, and protocol requirements.