About The Position

Clinical research takes brilliant investigators and innovative ideas—but it also takes someone who can keep all the moving pieces moving in the same direction. In this role, you’ll be at the center of clinical research operations, connecting teams across our 8 hospitals, affiliated medical schools, investigators, research teams, finance partners, and leadership. From coordinating clinical trial initiatives and tracking action plans to supporting research technology, meetings, finances, and regulatory activities, you’ll help build the infrastructure that allows research to grow across our health system. If you’re the person who loves a good tracker, catches the detail everyone else missed, and somehow always knows what needs to happen next—this could be your role.

Requirements

  • Strong project coordination, organization, and follow-through
  • Excellent written and verbal communication skills
  • Confidence working with spreadsheets, trackers, shared documents, calendars, and Microsoft Office tools
  • Strong attention to detail and documentation
  • Ability to work independently while collaborating with teams across a large organization
  • A customer-service mindset and the ability to build strong working relationships
  • High School Diploma or GED OR 2 years of applicable work experience

Nice To Haves

  • Bachelor’s Degree
  • 1+ year of experience in hospital operations, data analytics, business administration, project management, or a related field
  • Experience working with data, project tracking, research operations, or complex healthcare initiatives

Responsibilities

  • Coordinate clinical research projects, meetings, timelines, and follow-up across multiple hospitals and academic partners
  • Support investigators and research teams with operational needs, documentation, and study coordination
  • Help implement and maintain clinical research systems, including our Clinical Trials Management System and Epic/MyChart research tools
  • Maintain trackers, dashboards, action plans, issue logs, and other tools that keep research initiatives moving
  • Coordinate research meetings from start to finish—including agendas, materials, minutes, decisions, and follow-up
  • Support clinical trial invoice processing, financial tracking, and coordination with finance partners
  • Help standardize research workflows, policies, procedures, templates, and training materials across the health system
  • Prepare status updates, leadership briefings, reports, and other research documentation
  • Coordinate with hospital leaders, investigators, academic partners, research teams, and external stakeholders
  • Support system and facility licensure tracking, documentation, renewals, and regulatory follow-up

Benefits

  • 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
  • Deliver healthcare with heart.
  • Give people a reason to smile.
  • Put a little love in your work.
  • Be honest and real, but with compassion.
  • Bring some lagniappe into everything you do.
  • Forget one-size-fits-all, think one-of-a-kind care.
  • See opportunities, not problems – it’s all about perspective.
  • Cheerlead ideas, differences, and each other.
  • Love what makes you, you - because we do
  • You are welcome here.
  • LCMC Health is an equal opportunity employer. All qualified applicants receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.
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