Medical Scribe

Delricht Research • New Orleans, LA

1d • Onsite

About The Position

DelRicht Research is seeking a Clinical Research Coordinator 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
• This is an onsite Monday-Friday position.
• Candidates should be comfortable with a demanding schedule and able to maintain flexibility to support a busy clinic environment.
• Be self motivated! Energetic! Positive!
• Focus on providing exceptional patient care and creating a strong experience for every patient interaction
• Bring maturity, accountability, and follow-through to a fast-paced, high-volume team environment
• Believe in high quality and have a high standard of compliance and execution in daily work
• 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

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

• Patients are welcomed into a professional, supportive, and efficient clinic environment throughout their study participation
• Clinical visits are prepared for and carried out with strong attention to detail so study procedures and documentation requirements are completed accurately
• Site capacity is strengthened by helping the team manage a high volume of patient visits and related study activity
• Patient communication is handled consistently to support attendance, engagement, and continuity across scheduled trial visits
• Study-related information is maintained in a timely manner across required systems and records
• Clinic flow is supported through effective coordination with physicians, team members, and study stakeholders
• Sponsors, clients, and research partners receive responsive, professional communication and a strong onsite experience
• The site leadership team is supported by a coordinator who demonstrates accountability, sound judgment, and readiness to learn clinical research operations from the ground up

Benefits

• Medical Insurance, with generous employer paid contributions
• Dental and Vision Insurance
• Short and Long Term Disability and Group Life Coverage
• Paid Time Off that builds throughout your career with the company
• 401K (+ discretionary match/profit sharing)
• 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
• Professional Development Program tailored to each team members profess goals. Our quarterly goal-setting initiative is designed to challenge our team members to reach and exceed their potential!

What This Job Offers

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