RN Research Coordinator

1000 Wellstar Health System, Inc.•Marietta, GA

10d•Onsite

About The Position

How would you like to work in a place where your contributions and ideas are valued? A place where you can serve with compassion, pursue excellence and honor every voice? At Wellstar, our mission is simple, yet powerful: to enhance the health and well-being of every person we serve. We are proud to have become a shining example of what's possible when the brightest professionals dedicate themselves to making a difference in the healthcare industry, and in people's lives.

Requirements

Graduate from an approved school of nursing.
Bachelor's Degree BSN Preferred
Reg Nurse (Single State) or RN - Multi-state Compact
Minimum 5 years RN experience Required
Minimum 2 years Research experience
Hospital experience
Critical Care experience
Strong computer skills
good oral and written communication skills
excellent interpersonal and organization skills

Nice To Haves

Bachelor's Degree BSN

Responsibilities

Coordinates all facets of patient involvement in clinical trials.
Conducts all aspects of clinical trial, including consenting, using Good Clinical Practice, FDA, and Institutional guidelines.
Reviews patient chart for eligibility requirements and enrolls patient according to protocol guidelines.
Communicates with physician/office staff regarding scheduling protocol specific requirements.
Attends patient visits and gathers protocol-specific information when required.
Communicates drug doses, protocol requirements and modifications to physician and office staff as appropriate.
Coordinates dispersement of protocol provided drug therapy.
Ensures that Investigation Product chain-of-custody practices are instituted and documented.
Maintains accurate records for patients enrolled on clinical trials.
Communicates effectively with Research Assistants and other research staff.
Gathers appropriate source documentation.
Submits required documentation within designated time frame.
Provides proper documentation of eligibility, treatment and follow-up requirements.
Provides accurate research information to physicians and sponsors.
Maintains a current chart on each protocol patient.
Enters patient visits into clinical trial database.
Ensures regulatory guidelines are followed.
Prepares research charts for monitoring visits and audits and assists with visits as required.
Follows guidelines and timelines for reporting Adverse Events and Deviations.
Maintains current protocol with revisions, amendments and current IRB approved informed consent.
Ensures clinical trial and sponsor-required training is completed.
Ensures that all training related to start-up of a clinical trial is accomplished, including attending Investigator Meetings when required.
Ensures that ongoing training during the course of a clinical trial is completed.
Facilitates ongoing training for other team members, including investigators.
Maintains current Human Research Participant Protection and Hazardous Material training.
Assists with other departmental functions.
Attends committee meetings as required.
Attends functional team meetings and disseminates information.
Assists with regulatory and billing functions, when required.
Responsible for additional projects, as directed by the manager.