Clinical Research Coordinator East Jefferson General Hospital

Position: Clinical Research Coordinator (Full-time; Days) - East Jefferson General Hospital
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.💼 What You’ll Do 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 What Makes You Great in This Role You’re incredibly organized and details rarely get past youYou 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🧠 What You Bring 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📋

Minimum Requirements Bachelor’s Degree in a related field2+ years of experience in post-graduate medical education and medical research studies🎯 Why This Role Matters 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.💙 Coordinate the details. Support the science. Help move medicine forward.

WORK SHIFT:

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

About East Jefferson General Hospital East Jefferson General Hospital, a landmark of LCMC Health’s incredible community of…