Oncology Research Consultant RN - Epic Treatment Plan Intake Form Builder

American Addiction Centers • Charlotte, NC

4d • Onsite

About The Position

This position is for a study start-up (SSU) EPIC Intake Form Builder role, which plays a key role in ensuring the successful activation and coordination of clinical trials that advance cancer care and treatment options. Atrium Health Levine Cancer Institute is located in Charlotte, NC, and serves as a leading provider of comprehensive cancer care for patients across the region. We offer innovative, state-of-the-art oncology services, including prevention, diagnosis, treatment, and survivorship support across a wide range of cancer types. Our multidisciplinary approach brings together expert physicians, advanced practice providers, nursing, and supportive care teams to deliver personalized treatment plans. Services include medical, surgical, and radiation oncology, clinical trials, infusion therapy, and supportive programs such as navigation, genetic counseling, and survivorship care.

Requirements

• 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.
• CPR certification required.

Nice To Haves

• Bachelor's Degree in Nursing or Master's Degree in Nursing or other health/science degree concentration preferred.
• 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.
• Able to manage multiple tasks producing high quality work.
• Able to work across multiple teams within the CTO and other LCI departments.
• Self-starter and results driven.
• Strong attention to details.
• Strong organizational skills.

Responsibilities

• 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.

Benefits

• 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

What This Job Offers

• Job Type: Full-time
• Career Level: Senior