Medical Assistant, Clinical Research

DelRicht Research•Hendersonville, TN

2d•$60,000 - $65,000•Onsite

About The Position

DelRicht Research conducts clinical trials to give patients access to new treatment options and help new medications and medical devices gain FDA approval. The Medical Assistant, Clinical Research helps create a welcoming clinic environment and complete patient visits accurately and efficiently in accordance with clinical trial protocols and site expectations. The role supports participant screening, enrollment, retention, and completion of scheduled study visits, while prioritizing participant safety and timely follow-through. It also involves accurate, timely clinical data entry and clear communication with patients, physicians, and other stakeholders. The position is full-time, on-site in Hendersonville, Tennessee, with occasional travel to Smyrna, Tennessee. The schedule is Monday through Friday, 8 a.m. to 5 p.m., for 40 or more hours per week. Base salary is $60,000–$65,000, with estimated total annual compensation of $66,000–$75,000 including potential quarterly performance- and productivity-based bonuses; total compensation is not guaranteed.

Requirements

At least one year of professional experience; a medical or clinical background is ideal.
Clear communication, sound judgment, and the ability to find solutions when priorities shift or situations are uncertain.
Careful attention to detail and organizational skills to manage competing demands.
Ability to learn study protocols, systems, and clinical workflows quickly.
Patient-focused approach and willingness to collaborate with colleagues.
Comfort performing blood draws, EKGs, vital signs, and charting during patient visits; training is available.

Nice To Haves

A bachelor’s degree from an accredited college or university is preferred, but not required.
A medical or clinical background is ideal.

Responsibilities

Create a welcoming clinic environment where patients feel comfortable throughout their visits.
Complete patient visits efficiently and accurately, following clinical trial protocols and site expectations.
Carry out patient screening, enrollment, and retention activities with attention to safety, detail, and timely follow-through.
Guide participants through study requirements and help them attend and complete scheduled visits.
Record clinical data accurately and submit it on time in required systems.
Keep patients, physicians, and other stakeholders informed through clear, timely communication.
Perform blood draws, EKGs, vital signs, and charting during patient visits.