Part-Time Clinical Research Nurse

About the role

This role is an on-site Clinical Research Nurse position supporting an oncology clinical trial at a dedicated research site in Mobile, AL. The nurse will contribute to all aspects of trial execution, including patient pre-screening, data entry and verification, electronic diary compliance, lab kit support, participant follow-up, and study visit preparation.

Responsibilities

• Support all clinical and operational tasks associated with an oncology research trial at the site.
• Pre-screen patients for eligibility and review charts to confirm inclusion and exclusion criteria.
• Perform accurate and timely data entry into clinical trial databases and electronic systems.
• Verify data for completeness, accuracy, and consistency, and resolve data queries as needed.
• Monitor and support participant compliance with electronic diaries (e-diaries).
• Prepare lab kits and support specimen collection, processing, and documentation in accordance with protocol.
• Collaborate with clinical research coordinators and other site staff to ensure smooth trial operations.
• Utilize electronic medical records (EMR) systems to review and document participant information.
• Aid in recruitment activities to identify and enroll eligible participants.
• Adhere to Good Clinical Practice (GCP) guidelines, HIPAA regulations, and site-specific standard operating procedures.
• Maintain meticulous attention to detail in all aspects of documentation and trial conduct.
• Contribute to a fast-paced research environment by prioritizing tasks and meeting protocol timelines.

Requirements

• Minimum of 2 years of experience working as a Clinical Research Nurse.
• Demonstrated experience in clinical research, preferably in oncology trials.
• Proficiency with electronic medical records (EMR) systems.
• Strong data entry skills with a focus on accuracy and completeness.
• Experience in patient pre-screening and chart review for clinical trials.
• Knowledge and application of Good Clinical Practice (GCP) guidelines.
• Training in HIPAA regulations and patient privacy requirements.
• Experience in managing e-diary compliance and supporting participants in using electronic tools.
• Experience verifying clinical trial data and resolving queries.
• Strong organizational skills and attention to detail in a fast-paced environment.
• Ability to work full-time (40 hours per week) for the duration of a 7-month contract.