Clinical Research Coordinator I

Tulane University • New Orleans, LA

2d

About The Position

The Clinical Research Coordinator coordinates and conducts day-to-day operations for ongoing hematology-oncology studies. The role requires in-depth knowledge of protocol requirements and good clinical practices established by federal regulations. As the primary resource for protocols, the coordinator serves as a liaison 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. The position is also responsible for data and source documentation, adverse event reporting, and maintaining complete regulatory files.

Requirements

• Bachelor’s degree in public health or another science area, or current Louisiana licensure as an RN at the time of hire, or current state licensure as an LPN at the time of hire.
• Three years of clinical research experience conducting research and clinical trials, including recruitment and coordination of research activities.
• In-depth knowledge of protocol requirements and good clinical practices as set forth by federal regulations.
• Proficiency with software programs, including database management (e.g., Access), presentation packages (e.g., PowerPoint), spreadsheets (e.g., Excel), and advanced word processing (e.g., Word).
• Excellent organizational, interpersonal, communication, and analytical skills.
• Highly detailed and organized, with an excellent work ethic.
• 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 the day-to-day operations of ongoing hematology-oncology studies.
• Serve as the primary protocol resource and liaison between patients, investigators, the research team, the Institutional Review Board, and sponsors.
• Screen, enroll, and follow study patients.
• Ensure 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.
• Organize, prioritize, and schedule work assignments.
• Maintain confidentiality in all work performed.

What This Job Offers

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