Oncology Research Consultant RN - EPIC Treatment Plan Intake Form Builder Atrium Health

Advocate Aurora Health • Charlotte, NC

76d • $43 - $64 • Hybrid

About The Position

This role will support the EPIC intake, drug build and treatment validation process, which are essential tasks for clinical trial activation. In addition, this role will collaborate with key stakeholders to ensure EPIC treatment builds are accurately built to comply with protocol requirements and institutional billing standards.

Requirements

• Must hold a valid applicable state 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.

Responsibilities

• Competently fulfills the job responsibilities of the Oncology Research Coordinator.
• 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.
• 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.

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: Mid Level
• Industry: Hospitals
• Education Level: Bachelor's degree