Regulatory Administrative Assistant

Delricht Research • New Orleans, LA

8d

About The Position

Would you love to be a part of the cutting edge of healthcare and science innovation? Do you want to be an influential part of a rapidly growing team? Are you looking for a position that has opportunities for professional growth? If the answer is yes, then DelRicht Research might be the right opportunity for you!

Who We Are
DelRicht is a clinical research company dedicated to providing an excellent customer experience to all patients that participate in our clinical trials. Our clinical trials provide new treatment options for our patients and ultimately our goal is to get new medications and medical devices FDA approved! We hold our team members to a high standard of excellence and are looking for energetic, positive, quick learners to be a part of our team. Presently our network stretches across 33 sites throughout the United States in 18 states.

DelRicht Research has been recognized as a Top Workplace in 2023, 2024, and 2025! This is a testament to our unwavering commitment to creating an exceptional work environment that fosters growth, collaboration, and employee satisfaction.

Regulatory Administrative Assistant Main Objective: The Administrative Assistant will assist our Regulatory Team with providing high level, centralized support organizing and running the busy day-to-day operations of our numerous clinical research sites throughout the US.

Requirements

• Email management
• Excellent with Apple computers and all Google Workspace applications
• Be self motivated! Energetic! Positive!
• Be remarkably organized
• Be skilled at problem solving
• Accept ownership of tasks from inception through completion and assume responsibility for personal success
• Love efficiency and continuously look for ways to do more with less, improve processes and come in under budget
• B.S or B.A from any accredited university or equivalent work experience (1-2 years professional experience)
• 1+ years administrative and/or assistant experience is a plus
• Exceptional organizational skills

Nice To Haves

• Clinical Research or Regulatory experience is not required but always a plus!
• Coffee drinkers preferred. Tea drinkers accepted.

Responsibilities

• Help complete documents required to initiate new clinical research trials
• Ensure quality documentation and training throughout each clinical trial, including processing clinical trial amendments
• Maintain site staff certifications
• Respond to client inquiries regarding requests for information
• Support clinical research sites and team cohesion by providing clear and consistent communication regarding clinical trial activities
• Assist in the initial set up of new clinical trial Sites
• Monitor and maintain equipment used for clinical trials

Benefits

• Medical, Dental, Vision, Short & Long Term Disability and Life Insurance (group rates!)
• Generous Paid Time Off that builds throughout your career with the company
• No nights or weekends
• 401K (+ discretionary match/profit sharing)
• Exceptional quarterly bonus plan that clearly outlines your bonus potential per quarter and giving the team the visibility and control to maximize earnings by hitting team goals
• Job Type: Full-time, 40+hours

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Number of Employees: 11-50 employees