Clinical Research Coordinator I

Tulane University • New Orleans, LA

2d

About The Position

The Clinical Research Coordinator coordinates and conducts the day-to-day operations of ongoing hematology-oncology studies. The role requires in-depth knowledge of protocol requirements and good clinical practices established by federal regulations. Serving as a primary protocol resource, the coordinator liaises among patients, investigators, the research team, the Institutional Review Board, and sponsors. The coordinator screens, enrolls, and follows study patients, ensuring protocol compliance and effective monitoring of clinical trial subjects. Responsibilities also include data and source documentation, adverse event reporting, and maintaining complete regulatory files.

Requirements

• Bachelor’s degree in public health or another science area, or RN with current Louisiana licensure at the time of hire, or LPN with current state licensure at the time of hire.
• Three years of clinical research experience conducting research and clinical trials, including recruitment and coordinating research activities.
• In-depth knowledge of protocol requirements and good clinical practices as set forth by federal regulations.
• Excellent organizational, interpersonal, and communication skills.
• Proficiency with software including database management (e.g., Access), presentation packages (e.g., PowerPoint), spreadsheets (e.g., Excel), and advanced word processing (e.g., Word).
• Highly detailed and organized.
• Excellent work ethic and analytical skills.
• Ability to multitask and work independently.
• Ability to maintain confidentiality in all work performed.

Nice To Haves

• Master’s degree in clinical research or public health.
• Certified Clinical Research Coordinator.
• Clinical research experience in hematology, bleeding, and clotting disorders.

Responsibilities

• Coordinate and conduct day-to-day operations of ongoing hematology-oncology studies.
• Serve as a primary protocol resource and liaison between patients, investigators, the research team, the Institutional Review Board, and sponsors.
• Screen, enroll, and follow study patients while ensuring protocol compliance and effective monitoring of clinical trial subjects.
• Maintain data and source documentation, report adverse events, and maintain complete regulatory files.
• Coordinate research activities, including generating study recruitment, intervention, and follow-up reports.
• Train study staff and organize, prioritize, and schedule work assignments.
• Maintain confidentiality in all work performed.

What This Job Offers

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