Regulatory Coordinator

DelRicht Research • Metairie, LA

2d • Onsite

About The Position

DelRicht Research is a clinical research site network dedicated to providing an excellent customer experience to patients participating in clinical trials. Its trials provide new treatment options, with the goal of getting new medications and medical devices FDA approved. The network spans 33 sites across 18 states.

The Regulatory Coordinator manages documentation submissions to support timely initiation of new clinical research trials, supports quality documentation and training processes, and delivers timely and accurate clinical trial amendment notices. The role also maintains site staff certifications and supporting documentation; researches and responds to client inquiries; communicates forthcoming trial activities and amendments to research locations; assists with setting up new clinical trial sites; and monitors and maintains equipment used for clinical trials.

This is a full-time, on-site position in Metairie, Louisiana, with a stated schedule of 40+ hours per week. Starting compensation is $50,000.

Requirements

• At least two years of administration or project management experience.
• Exceptional organizational skills and strong attention to detail.
• Advanced problem-solving skills and adaptability, with the ability to follow tasks through to completion.
• Proficiency with Apple computers, Google Workspace applications, and management of other relevant technical systems.
• Bachelor's degree from an accredited university or three years of equivalent professional experience in healthcare, research, or other compliance functions.
• A self-motivated, positive approach to work and collaboration.

Nice To Haves

• Coffee drinkers preferred; tea drinkers accepted.

Responsibilities

• Manage the documentation submission process to ensure timely initiation of new clinical research trials.
• Support quality documentation and training processes for clinical trials.
• Deliver timely and accurate clinical trial amendment notices.
• Maintain site staff certifications and supporting documentation.
• Research and respond to client inquiries or requests for information related to clinical trials.
• Communicate forthcoming trial activities and amendments to clinical research locations.
• Assist with the initial setup of new clinical trial sites.
• Monitor and maintain equipment used for clinical trials.

Benefits

• Medical insurance with generous employer-paid contributions.
• Dental and vision insurance.
• Short- and long-term disability coverage and group life coverage.
• Paid time off that builds throughout the employee's career with the company.
• 401(k) with discretionary match/profit sharing.
• Quarterly bonus plan with stated bonus potential and team goals.
• Professional Development Program tailored to each team member's professional goals.

What This Job Offers

• Job Type: Full-time