Clinical Research Coordinator University Medical Center

Your job is more than a job. Help Turn Today’s Research Into Tomorrow’s Care Every medical breakthrough starts somewhere—and clinical trials are where promising ideas meet real-world patient care. As a Clinical Research Coordinator, you’ll help bring clinical trials to life by keeping studies organized, compliant, accurate, and moving forward. You’ll work alongside research teams, study sponsors, and participants to coordinate everything from enrollment and documentation to investigational supplies and follow-up visits.

If you love science and a good checklist, can keep a dozen details moving without losing track of one, and want your work to contribute to the future of healthcare, this could be the role for you.

• Coordinate clinical trials from study planning through ongoing trial activities
• Review study requirements and help develop timelines, workflows, and trial plans
• Support research participant enrollment and follow-up visits
• Complete case report forms and maintain accurate source documentation
• Track investigational medications, devices, and study supplies from receipt through return
• Prepare and submit regulatory documents and study correspondence on time
• Organize research workflows, schedules, records, and trial documentation
• Communicate with study sponsors, research participants, and internal research teams
• Help troubleshoot operational issues and keep studies moving according to protocol
• Protect participant privacy and maintain confidential research records

• You’re incredibly organized and details rarely get past you
• You can manage multiple deadlines without losing sight of the bigger picture
• You enjoy working at the intersection of science, healthcare, and people
• You’re comfortable following detailed protocols while knowing when something needs to be escalated
• You communicate confidently with research participants, study sponsors, and clinical teams
• You understand that in clinical research, documentation matters
• You’re curious, observant, and always thinking a few steps ahead

• Strong organizational and time-management skills
• Excellent communication and interpersonal abilities
• Careful observation and assessment skills
• Confidence working with computers, research documentation, and electronic systems
• Ability to communicate with study sponsors and research participants
• Experience operating clinical equipment such as ECG machines, spirometers, stadiometers, and scales
• Basic phlebotomy and vital sign skills are a plus

• Bachelor’s Degree in a related field
• 2+ years of experience in post-graduate medical education and medical research studies

Clinical trials depend on more than innovative treatments and great ideas. They depend on careful coordination, accurate documentation, participant support, regulatory compliance, and someone making sure all the pieces come together. That’s where you come in. Your work helps research teams answer important questions today that could change how patients are cared for tomorrow.

Days (United States of America)

LCMC Health is a community. Our people make health happen. While our NOLA roots run deep, our branches are the vessels that carry our mission of bringing the best possible care to every person and parish in Louisiana and beyond and put a little more heart and soul into healthcare along the way. Celebrating authenticity, originality, equity, inclusion and a little “come on in” attitude is the foundation of LCMC Health’s culture of everyday extraordinary.

University Medical Center, a world class academic medical center in LCMC Health’s incredible community of care, is the largest medical training center for healthcare professionals…