Limited Term Medical Assistant

DelRicht Research • Baton Rouge, LA

6d • Onsite

About The Position

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 for 2023, 2024, 2025, and 2026!! This is a testament to our unwavering commitment to creating an exceptional work environment that fosters growth, collaboration, and employee satisfaction.

Requirements

• At least 1 year of professional work experience
• Comfort working in a clinic environment and learning clinical research workflows
• Strong time management, reliability, and follow-through
• Tech-savvy and comfortable learning new systems
• Ability to take direction, stay organized, and support a team through changing priorities
• A professional, flexible, and team-oriented approach
• Medical Assistant certification, LPN background, or similar healthcare training
• Bachelor’s degree or equivalent experience, especially for candidates without a clinical certification or licensure
• Experience supporting patient visits, clinical operations, or healthcare documentation
• Interest in clinical research, healthcare, or a future medical career
• Be self motivated! Energetic! Positive!
• Bring professionalism, maturity, and strong personal accountability to a fast-paced clinical environment
• Be highly dependable and able to maintain focus in a role that requires precision and trust
• Be remarkably organized
• Be skilled at problem solving, planning and being proactive
• Accept ownership of tasks from inception through completion and assume responsibility for personal success

Responsibilities

• Support clinical research visits across multiple studies in a clinic setting
• Prepare study medication and coordinate handoff to the blinded team as needed
• Help create structure and stability during busy or changing visit schedules
• Follow study protocols, clinic processes, and documentation expectations accurately
• Communicate clearly with teammates and help the team adapt when priorities shift
• Maintain professionalism, timeliness, and reliability in a fast-paced clinical environment
• Balance unblinded study responsibilities with the ability to support broader CRC work across general medicine and other site needs

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level