Registered Nurse (RN) - Oncology - $32-58 per hour New

Atrium Health Charlotte is seeking a Registered Nurse (RN) Oncology for a nursing job in Charlotte, North Carolina.

Job Description & Requirements

• Specialty: Oncology
• Discipline: RN
• Start Date: ASAP
• Duration: Ongoing
• Employment Type: Staff

Overview

Our Commitment to You:​

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Advocate Health offers a comprehensive suite of Total Rewards: benefits and well-being programs, competitive compensation, generous retirement offerings, programs that invest in your career development and so much more – so you can live fully at and away from work, including:​

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Compensation​

Base compensation listed within the listed pay range based on factors such as qualifications, skills, relevant experience, and/or training​

Premium pay such as shift, on call, and more based on a teammate's job​

Incentive pay for select positions​

Opportunity for annual increases based on performance​

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Benefits and more​

Paid Time Off programs​

Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability​

Flexible Spending Accounts for eligible health care and dependent care expenses​

Family benefits such as adoption assistance and paid parental leave​

Defined contribution retirement plans with employer match and other financial wellness programs​

Educational Assistance Program​

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Salary:  $90,064.00 - $135,096.00

Job Summary

Conducts and develops all aspects of clinical, regulatory, business, and other research- related activities and documentation for clinical trials on behalf of the Levine Cancer Institute, following industry standards and applicable regulations including FDA/OHRP guidance, GCP and ICH.

Essential Functions
 

• Competently fulfills the job responsibilities of the Oncology Research Coordinator, and:
• Assists Principal Investigator and team in evaluating feasibility of research studies.
• Develops study budget in collaboration with team.
• Coordinates documentation for regulatory requirements.
• Coordinates trial-related activity of patients on protocols.
• Coordinates, follows, and evaluates patient participation in clinical trials to ensure compliance with the protocol.
• Coordinates protocol-specific clinical tasks including patient assessment, eligibility screening, symptom management, toxicity assessment, and monitoring of responses.
• Coordinates protocol-specific scheduling of tests and specimen collection across LCI locations.
• Monitors and reports significant study events including adverse events and protocol amendments, activity, status, and closures.
• Performs required study procedures, collects data, analyzes data and makes decisions regarding the clinical research study conduct, including initial screening, assessment, care, reassessment and modification of care in consultation with PI and team.
• Assists in data analysis and drafting of clinical study reports.
• Develops, updates and/or implements standard operating procedures (SOPs).
• Serves as a team leader.
• Serves as the key resource for Principal Investigator, physicians and research team and acts as the primary liaison with sponsors to facilitate study initiation, execution and termination.
• Ensures accurate and timely data collection, submission, and query resolution.
• Coordinates protocol-level documentation to ensure regulatory and institutional compliance.
• Educates patients and families about research studies, treatments, side effects and follow-up, as appropriate.
• Coordinates protocol activities across Levine Cancer Institute.
• Collaborates with investigators through attendance at Section meetings, conferences, and other meetings.
• Acting on behalf of the sponsor for Atrium Health Wake Forest Baptist Comprehensive Cancer Center (AHWFBCCC), facilitates the completion of Investigator-Initiated Research (IIR) project development in collaboration with the Principal Investigator, Biostatistics, QA Monitoring, Pharmacy, Regulatory, Clinical and Data Project Management, Finance, Contracts, external funding entities and other key sponsor stakeholders
• · Edits sections of IIR protocols after first draft is completed
• · Writes informed consent forms for IIR protocols
• · Writes operational manuals for IIR protocols, in collaboration with stakeholders
• · Manages questionnaires/surveys (creation and/or obtaining permissions, translation, etc) for use in IIR projects
• · Facilitates protocol development meetings
• · Serves as the key project contact for external funding entities during the development phase
• · Coordinates stakeholder review of external funder/vendor contract drafts in collaboration with Contracts
• · Coordinates and facilitates Site Initiation Visit training for IRB-approved IIR projects
• · Collaborates with the Regulatory and Compliance team on IRB/FDA submissions and review
• · Ensures relevant IIR documents are maintained in the regulatory binder
• · Facilitates IIR protocol amendments in collaboration with key stakeholders
• · Coordinates and leads applicable sponsor-led meetings with key stakeholders
• · Prepares agendas and minutes for IIR study team meetings
• · Reviews and assesses IIR protocol questions from study conduct sites and provides appropriate feedback or triaging
• · Assists with/facilitates amendments to LCI-sponsored clinical trials
• · Ensures contractual requirements with external collaborators are being met; writes and sends progress reports on IIR projects per funder requirements
• · Facilitates completion of Data and Safety Monitoring Committee reports for IIR clinical trials
• · Reviews, queries, and reports expedited safety event and deviation reports received from study conduct sites on IIR protocols
• · Creates and conducts applicable Site Initiation Visit and amendment training for study conduct sites
• · Assists in the development, improvement and review of Standard Operating Procedures and processes.
• · Provides educational and technical assistance to new IIR teammates including orientation and mentoring of new IIR teammates.

Physical Requirements
 

Primarily works in an office setting. Requires full range of body motion; sitting for extensive periods of time; walking, standing, reading, and writing/keyboarding. Occasionally lifts and carries items weighing up to 35 pounds. Requires corrected vision and hearing within normal range. Must speak and read/write clearly in English. Must be able to be mobile within the entire healthcare system and other locations that participate in LCI clinical trials.

Education, Experience and Certifications
 

Must hold a valid North Carolina or South Carolina (as applicable) Board of Nursing license. Bachelor's Degree and 3 years of clinical research experience with a pharmaceutical company or Contract Research Organization or equivalent experience required; or Master's Degree and 2 years of clinical research experience with a pharmaceutical company or Contract Research Organization or equivalent experience required; or a minimum of 6 years clinical research experience with a pharmaceutical company or Contract Research Organization or equivalent experience required with no degree. Bachelor's Degree in Nursing or Master's Degree in Nursing or other health/science degree concentration preferred. CPR certification required. Previous experience in a healthcare setting preferred, especially cancer care and/or clinical research. Certification in clinical research (SoCRA, ACRP, RAPS, etc.) preferred. Supervisory experience preferred.

Additional Training and Certifications

· Ability to review and understand all aspects of a clinical research protocol

· Experience in serious adverse event reporting

· Clinical experience in Oncology preferred

· Collaborative attitude, with excellent verbal and written communication skills

· Organized, with ability to follow through, track, and follow-up on numerous ongoing initiatives

· Self-motivated and deadline-oriented, able to multi-task and function autonomously

Atrium Health Charlotte Job ID #1​5​2​2​7​1. Posted job title: Oncology Research Consultant- RN - Atrium Health LCI

About Atrium Health Charlotte

Headquartered in Charlotte, NC, Atrium Health is now part of Advocate Health, the third-largest nonprofit, integrated health system in the United States, which was created from the combination with Advocate Aurora Health. In the Southeast Region, Atrium Health provides care under the Atrium Health name in Charlotte, NC, Atrium Health Wake Forest Baptist name in the Winston-Salem, NC, region, as well as Atrium Health Navicent and Atrium Health Floyd in Georgia and Alabama. Together, we are committed to providing equitable care for all. Annually, Advocate Health provides nearly $5 billion in community benefits.

Atrium Health Wake Forest Baptist

Atrium Health Wake Forest Baptist is a pre-eminent academic health system based in Winston-Salem, North Carolina. Atrium Health Wake Forest Baptist is part of Advocate Health, which is headquartered in Charlotte, North Carolina, and is the fifth-largest nonprofit health system in the United States, created from the combination of Atrium Health and Advocate Aurora Health. Atrium Health Wake Forest Baptist's two main components are an integrated clinical system - anchored by Atrium Health Wake Forest Baptist Medical Center, an 885-bed tertiary-care hospital in Winston-Salem - that includes Brenner Children's Hospital, five community hospitals, more than 300 primary and specialty care locations and more than 2,700 physicians; and Wake Forest School of Medicine, the academic core of Atrium Health Enterprise and a recognized leader in experiential medical education and groundbreaking research that includes Wake Forest Innovations, a commercialization enterprise focused on advancing health care through new medical technologies and biomedical discovery.

Atrium Health Navicent

Atrium Health Navicent is the leading provider of healthcare in central and south Georgia and is committed to its mission of elevating health and well-being through compassionate care. Atrium Health Navicent is part of Advocate Health, which is headquartered in Charlotte, North Carolina, and is the third-largest nonprofit health system in the United States, created from the combination of Atrium Health and Advocate Aurora Health. Atrium Health Navicent provides high-quality, personalized care in 53 specialties at more than 50 facilities throughout the region. As part of the largest, integrated, nonprofit health system in the Southeast, it is also able to tap into some of the nation's leading medical experts and specialists with Atrium Health, allowing it to provide the best care close to home - including advanced innovations in virtual medicine and care. Throughout its 125-year history in the community, Atrium Health Navicent has remained dedicated to enhancing health and wellness for individuals throughout the region through nationally recognized quality care, community health initiatives and collaborative partnerships. It is also one of the leading teaching hospitals in the region, helping to ensure viability for rural health care for the next generation. 

Atrium Health Floyd

Atrium Health Floyd Medical Center is a 304-bed, full-service hospital located in Rome, Georgia. Serving as the main campus for Atrium Health Floyd, this hospital provides a certified Chest Pain Center, a designated Bariatric Surgery Center of Excellence and a Breast Imaging Center of Excellence. Atrium Health Floyd also is home to a state-designated Level II Trauma Center and a Level III Neonatal Intensive Care Unit, and has specialty centers for pediatrics, and wound care and hyperbaric therapy.

Benefits

• Medical benefits
• Vision benefits
• Dental benefits
• Life insurance
• 401k retirement plan
• Health savings account