Be a FWD Research Site.
Are you ready to expand your practice and bring cutting-edge treatment options to your patients? Our Be a FWD Site page is designed for healthcare providers and institutions eager to make a real impact through clinical research. By partnering with FWD Clinical Research, you’ll gain access to our network and be provided with resources to successfully navigate the industry and excel at operating your clinical trial site.
Imagine elevating your practice with the latest advancements in medicine, improving patient outcomes, and contributing directly to the future of healthcare. As a FWD research site, you’re not just joining a network; you’re becoming part of a movement that pushes the boundaries of what’s possible in patient care.
Access to Innovative Studies
Gain early access to cutting-edge clinical trials that bring the latest treatments and technologies to your patients.
Enhance Professional Development
Collaborate with top researchers, industry leaders, and pharmaceutical companies, elevating your site’s reputation and expanding your expertise.
Grow Your Practice
Position your site at the forefront of medical innovation, increasing visibility and creating new revenue streams through clinical research participation.
Research Site Development
At FWD Clinical Research, we offer a comprehensive and integrated approach to research site development for healthcare practices, provider groups, and institutions. Our experienced operational team will work closely with you to create a customized site development plan that seamlessly aligns with your practice's workflow.
Our services are provided:
Development Plan & SOPs – Tailored site development and standard operating procedures to ensure smooth integration.
Study Identification – Matching your site with appropriate clinical trials.
Budget and Contract Negotiations – Securing favorable terms for your participation in studies.
Site Start-Up – Ensuring all processes are in place for a successful launch.
Patient Recruitment – Assisting with strategies to recruit and retain study participants.
Invoicing – Handling study-related billing and financial management.
Staff Training – Training your in-office staff on clinical trial procedures.
