Research Assistant

Headlands Research•Detroit, MI

2d•Onsite

About The Position

At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion. Headlands Research – Metro Detroit is a leading clinical research site dedicated to advancing medical innovation and expanding access to clinical trials. Strategically located in the Detroit metro area, we serve a large and diverse population while conducting multi-therapeutic and general medicine studies. We are committed to ensuring all participants have access to cutting-edge therapies, helping to shape a healthier future for the communities it serves. We’re seeking a Clinical Research Assistant for our clinical research site located in Detroit, MI. As a Clinical Research Assistant, you’ll work side-by-side with experienced Clinical Research Coordinators, Investigators, and cross-functional teams to support all aspects of clinical trial execution—from subject screening to data entry. Your work will directly contribute to the success of new treatments in development. Want to be a part of a growing company that’s making a difference in our world? Look no further than Headland Research! You’ll enjoy a friendly and exciting culture with opportunities for growth and advancement.

Requirements

Familiarity with medical terminology and basic laboratory procedures
Prior experience providing direct hands-on patient care
Comfortable using multiple electronic data entry systems
Strong attention to detail, time management, and ability to work in a fast-paced, regulated environment
Excellent interpersonal skills—you’ll be interacting with participants, providers, and sponsors
Passion for improving patient outcomes through research

Nice To Haves

Clinical research experience preferred

Responsibilities

Assist research coordinators in conducting clinical trial visits in compliance with study protocols
Collect and record vital signs , make study-related phone calls, and document data in electronic systems
Support subject screening, enrollment , and follow-up processes
Review and verify study documentation for accuracy and completeness
Maintain close communication with coordinators, investigators, and study participants