RN Research Coordinator

Wellstar Health Systems; Marietta (GA); On-site; USD 60,000 - 85,000; Full time

Job summary

Wellstar Health System in Georgia seeks a Research Coordinator to manage clinical trials. You will identify potential patients, assess eligibility, enroll participants, coordinate therapy initiation, and maintain records in the Clinical Trials Office.

You will ensure protocol adherence, work with physicians and staff, document adverse events, and support audits. A BSN and RN license are required, with at least 5 years nursing and 2 years research experience.

Qualifications

• Graduate from an approved school of nursing.
• Bachelor's Degree in Nursing (BSN) preferred.
• Hold RN license (state or multi-state).
• Minimum 5 years RN experience.
• Minimum 2 years research experience.
• Critical Care experience preferred.

Responsibilities

• Coordinate all facets of patient involvement in clinical trials.
• Conduct trials per Good Clinical Practice and FDA guidelines.
• Assess eligibility and enroll patients per protocol.
• Communicate dosing and protocol requirements to care teams.
• Maintain trial records and documentation for audits.
• Facilitate training and regulatory compliance.

Skills

RN experience

Computer skills

Communication skills

Interpersonal skills

Education

BSN degree

RN license

Job description

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.

Work ShiftDay (United States of America)Job Summary:

The Research Coordinator has general responsibility for managing clinical trials for the Clinical Trials Office of the WellStar Health System. This includes responsibility for identifying potential study patients; ascertaining patient eligibility for clinical trials; coordinating, evaluating, and following patients in clinical trials; coordinating therapy initiation and continuation; taking call for issues related to clinical trials; completing and filing necessary forms with internal and external departments and agencies as necessary; and maintaining records for patients enrolled in clinical trials.

Core Responsibilities and Essential Functions:

• - 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.

Required Minimum Education:

Graduate from an approved school of nursing. Required andBachelor's Degree BSN PreferredRequired Minimum License(s) and Certification(s):All certifications are required upon hire unless otherwise stated.Reg Nurse (Single State) or RN - Multi-state CompactAdditional License(s) and Certification(s):Required Minimum Experience:Minimum 5 years RN experience Required andMinimum 2 years Research experienceHospital experienceCritical Care experienceRequired Minimum Skills:Strong computer skills;good oral and written communication skills;excellent interpersonal and organization skills.Join us and discover the support to do more meaningful work-and enjoy a more rewarding life. Connect with the most integrated health system in Georgia, and start a future that gives you more.