LPN - Research

Cardiovascular Institute of the South•Houma, LA

About The Position

As a Licensed Practical Nurse (LPN) – Research , you will play a critical role in the coordination and execution of clinical research studies. Your responsibilities will include subject recruitment, regulatory compliance, data and documentation management, patient care, and coordination with investigators and support teams. This position requires strong attention to detail, the ability to work independently, and a passion for advancing patient outcomes through clinical research.

Requirements

High school diploma or equivalent required
Graduate from an accredited vocational-technical school
Current Louisiana LPN license
Minimum 1 year of experience as an LPN
BLS certification required
Strong communication, documentation, and organizational skills
Understanding of HIPAA regulations and commitment to maintaining confidentiality
Comfortable with EMR systems and electronic data entry

Responsibilities

Subject Recruitment and Screening: Prescreen and review medical records for eligibility Contact and schedule qualified study participants Present study information to both patients and healthcare professionals Monitor enrollment goals and adjust recruitment strategies accordingly
Study Initiation and Coordination: Understand all aspects of assigned protocols, including inclusion/exclusion criteria Collaborate with the Principal Investigator to develop recruitment and management strategies Prepare protocol worksheets, informed consent materials, and follow-up tools
Patient Enrollment and Consent: Confirm eligibility using source documents and external records Educate patients on protocol, risks/benefits, and follow-up procedures Obtain and document informed consent appropriately
Study Activity Management and Compliance: Monitor adherence to protocol and subject compliance Assist investigators in assessing response to therapy and reporting abnormal labs Manage investigational therapy administration and documentation Coordinate with pharmacies, labs, and ancillary departments
Data and Documentation: Record data accurately in the appropriate electronic or paper-based platforms Maintain source documentation and communication logs Schedule and prepare for monitoring visits and respond to sponsor queries Submit documentation to IRBs, including adverse events, protocol amendments, and study updates
Safety Monitoring and Reporting: Assist investigators in identifying and reporting adverse events Record, report, and follow up on all serious adverse events per protocol
Regulatory and Audit Compliance: Ensure all regulatory documentation is complete and accessible Coordinate and prepare for internal and external audits and inspections Serve as the point of contact for sponsors, auditors, and regulators
Close-Out and Reporting: Reconcile investigational products and prepare final documentation for sponsors and IRBs Audit and archive study files in accordance with FDA regulations
Training and Team Support: Assist in training and mentoring support staff and volunteers Perform other duties as assigned to support the goals and mission of CIS

Benefits

Choice of three health insurance plans
Dental insurance coverage
Vision insurance coverage
401(k) with company match and profit-sharing plan
Company-paid short-term and long-term disability coverage
Company-paid life insurance for you and your family
Access to company-provided training and educational resources
Eligibility for annual merit-based performance increases
Accrued General Purpose Time (GPT)
Eight company-paid holidays
Special company events, including Christmas parties, Family Day, employee engagement activities, and Spirit Days
Complimentary Employee Assistance Program (EAP) for all employees and their dependents