Limited Term Clinical Research Coordinator - Immediate Start!

DelRicht Research•Mandeville, LA

6d•$50,000 - $58,000•Onsite

About The Position

We are seeking a Limited-Term Blinded Clinical Research Coordinator to support a GLP-1 clinical trial at our North Shore clinic. This is a full-time, temporary opportunity designed for individuals looking to gain hands-on clinical research experience while assisting a collaborative team in managing a busy study. The role involves close collaboration with the existing study team to support daily visits, blinded study activities, data uploads, and study documentation. No RN licensure is required, making it a potentially strong fit for those early in their clinical research careers who are organized, dependable, and eager to learn. This position is slated to last for approximately 12 weeks with the possibility of extension.

Requirements

At least one year of professional work experience, or relevant clinical experience.
A bachelor’s degree in any field is preferred; candidates with relevant hands-on clinical training or experience, including Medical Assistants or LPNs, may also be considered.
Clinical or clinical research experience is great, but we are open to candidates from other backgrounds who demonstrate strong judgment and a willingness to learn.
Strong communication, organization, and attention to detail.
Dependability and the ability to manage responsibilities in a fast-paced environment.
Flexibility, sound judgment, and a team-first approach.
Bring a positive, energetic, and self-motivated attitude every day.
Prioritize exceptional patient care and contribute to a welcoming, supportive environment.
Balance multiple tasks with focus and efficiency.
Take ownership of responsibilities from start to finish, demonstrating accountability and reliability.
Leverage prior patient care experience while building new skills in clinical research.
Stay coachable and eager to learn, as we value growth and team fit even more than years of experience.
Embrace collaboration with a can-do spirit.

Nice To Haves

Coffee drinkers preferred… tea drinkers accepted :)

Responsibilities

Support day-to-day study visits and blinded trial activities.
Assist the study team with uploads, paperwork, and other required documentation.
Help keep study activities organized and moving efficiently during screening, enrollment, and ongoing participant visits.
Coordinate closely with team members and respond to changing study priorities.
Follow study protocols, clinic procedures, and applicable research requirements.
Take on additional study support tasks as delegated by the team.