Medical Scribe

DelRicht Research•New Orleans, LA

58d•Onsite

About The Position

DelRicht Research is seeking a Medical Scribe to join our New Orleans team in an onsite, patient-facing role. This is an excellent opportunity for someone early in their career who is eager to build hands-on experience in healthcare, research, and patient care while working in a fast-paced clinical environment. This role is ideal for a candidate who is excited to learn from the ground up, take ownership of their work, and contribute to both the patient experience and the operational success of clinical trials. We are looking for someone who can thrive in a busy clinic setting, support a high volume of activity, and help the team expand capacity as new studies begin. If you are motivated by meaningful work, interested in the future of medicine, and ready to grow within a company that values development and internal advancement, we encourage you to apply.

Requirements

Bachelor’s degree from an accredited university
1-2 years of professional experience or demonstrated work maturity and accountability
Comfortable with a demanding schedule
Able to maintain flexibility to support a busy clinic environment
Self-motivated, energetic, and positive
Focus on providing exceptional patient care and creating a strong experience for every patient interaction
Maturity, accountability, and follow-through in a fast-paced, high-volume team environment
Belief in high quality and a high standard of compliance and execution in daily work
Remarkably organized
Skilled at problem solving, planning and being proactive
Accept ownership of tasks from inception through completion and assume responsibility for personal success

Nice To Haves

Experience or exposure in healthcare, patient-facing environments, or roles that build familiarity with medical terminology, HIPAA, charting, or clinic flow

Responsibilities

Support high-quality study execution and help expand site capacity in a busy clinical research environment.
Ensure patients are welcomed into a professional, supportive, and efficient clinic environment throughout their study participation.
Prepare for and carry out clinical visits with strong attention to detail so study procedures and documentation requirements are completed accurately.
Strengthen site capacity by helping the team manage a high volume of patient visits and related study activity.
Handle patient communication consistently to support attendance, engagement, and continuity across scheduled trial visits.
Maintain study-related information in a timely manner across required systems and records.
Support clinic flow through effective coordination with physicians, team members, and study stakeholders.
Ensure sponsors, clients, and research partners receive responsive, professional communication and a strong onsite experience.
Support the site leadership team by demonstrating accountability, sound judgment, and readiness to learn clinical research operations from the ground up.