Headlands Research, Inc.
Clinical Research Assistant New Lake Worth, FL
Headlands Research, Inc., Lake Worth, Texas, United States
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.
Clinical Research Assistant We’re seeking a
Clinical Research Assistant (RA)
for our clinical research site JEM Research Institute located in Lake Worth (Atlantis), FL. As an RA, you won’t just be supporting research—you’ll be helping shape the future of healthcare. This is an exciting opportunity for individuals with clinical experience who are ready to grow their skillset and income potential within the clinical research field.
The Role:
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.
Type: Full‑Time
Schedule: Monday‑Friday 8:00 am‑5:00 pm
Location: Onsite, Lake Worth, FL (remote or hybrid work not available)
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
Opportunities for professional development and career growth
A mission‑driven culture focused on advancing medicine and improving patient outcomes
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
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
As set forth in Headlands Research’s Equal Employment Opportunity policy, we do not discriminate on the basis of any protected group status under any applicable law.
#J-18808-Ljbffr
Clinical Research Assistant We’re seeking a
Clinical Research Assistant (RA)
for our clinical research site JEM Research Institute located in Lake Worth (Atlantis), FL. As an RA, you won’t just be supporting research—you’ll be helping shape the future of healthcare. This is an exciting opportunity for individuals with clinical experience who are ready to grow their skillset and income potential within the clinical research field.
The Role:
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.
Type: Full‑Time
Schedule: Monday‑Friday 8:00 am‑5:00 pm
Location: Onsite, Lake Worth, FL (remote or hybrid work not available)
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
Opportunities for professional development and career growth
A mission‑driven culture focused on advancing medicine and improving patient outcomes
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
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
As set forth in Headlands Research’s Equal Employment Opportunity policy, we do not discriminate on the basis of any protected group status under any applicable law.
#J-18808-Ljbffr