Partner With Us
At Headlands Research, we focus on ease of study start-up, delivery of the highest quality data, specialty/diverse participant access and expert participant retention for our CRO and Sponsor partners.
Fully owned Clinical Research Sites
- 500+ expert clinical research professionals spanning across the United States and Canada
- Embedded and dedicated site models allow maximum subject access
- Engaged KOLs and specialists for protocol review and feasibility input
- ICH GCP trained clinical staff
- Entirely electronic sites (eSource, eRegulatory, etc.) which provide our Sponsors/CROs with real-time access to study data
- Referral and EHR access through proprietary partnerships with large multi-specialty practices
- 5,000+ completed Phase I – IV studies
Integrated Model
- Centralized management and services team allows for a single point of contact during the feasibility, budgeting/contacting, start-up, etc. on your study
- Centralized operations to ensure consistency and performance
- Priority focus on quality data, expedited study start-up and participant retention
The Headlands Research Difference
We deliver of the highest quality data and participant access.
Our participant access:
- Site and physician partnership databases
- Unique access to diverse and specialty populations
- Hispanic/Latino
- African American
- Elderly (over 65+ years old)
- Pediatric and adolescent (under 18 years old)
- Large database(s) of healthy volunteers
- Clinical research centers located in large metropolitan areas with access to millions of potential participants
Advance Clinical Trials With Us
Choosing the correct sites is crucial to the success of your trial. Headlands Research sites are committed to efficient study start up, expedited enrollment and production of the highest quality data – all with the ease of a single point of contact. Please consider Headlands Research for your next trial: