Research Assistant

Headlands Research; Detroit (MI); On-site; USD 46,000 - 50,000; Full time

Benefits offered by this job

Health insurance

HSA/FSA

PTO

401(k) match

Holidays

Job summary

Headlands Research in Detroit, MI is seeking a Clinical Research Assistant to support study visits, data entry, and coordination on a busy clinical research site.

You will work alongside experienced Coordinators and Investigators to screen subjects, record vital signs, and ensure accurate documentation in electronic systems. The role is onsite with regular Monday–Friday hours and a competitive benefits package.

Qualifications

• Familiarity with medical terminology and basic laboratory procedures.
• Direct hands-on patient care experience is preferred.
• Clinical research experience is preferred.

Responsibilities

• Assist research coordinators in conducting clinical trial visits in compliance with study protocols
• Collect and record vital signs, make study-related 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

Skills

Medical terminology familiarity

Hands-on patient care

Clinical research experience

Job description

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.

Are you an experienced clinical research professional with a passion for advancing medicine? Join a leading, integrated clinical research network dedicated to high-quality data, patient-centered care, and innovation in clinical trials.

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. We offer the following generous benefits to our full-time employees:

Type: Regular Full-time Employee
Schedule: Mondays through Fridays, 8:00am - 5:00pm
Pay Range: $22-24/hr *Dependent upon relevant experience, certification, and education.
Location: Onsite in Southfield, MI (no capabilities for remote or hybrid work)
Reports to: Clinical Research Manager
Benefits: Our benefits package for full-time employees includes health insurance (medical, dental, and vision), Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA), Paid Time Off (PTO), a variety of disability, accident, and life insurance options, as well as many more.

What We Offer

• Competitive pay + annual performance incentives
• Medical, dental, and vision insurance
• 401(k) plan with company match
• Paid time off (PTO) and company holidays
• A mission-driven culture focused on advancing medicine and improving patient outcomes

You’ll be part of a growing, mission-driven organization that values its people. At our core, we’re committed to bringing innovative medical treatments to patients faster—while creating an environment where employees thrive. If you’re passionate about clinical research and ready to make a difference, we’d love to hear from you.

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

Requirements

• Familiarity with medical terminology and basic laboratory procedures [[required]]
• Prior experience providing direct hands-on patient care [[required/preferred]]
• Clinical research experience preferred
• 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

Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.

Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

Need Assistance?

Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact [e-mail] for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.