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 innovative studies and the opportunity to offer groundbreaking therapies—years ahead of public availability.
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 at no cost to you and include:
Development Plan & SOPs – Tailored site development and standard operating procedures to ensure smooth integration.
Protocol Feasibilities – Assessing the suitability of clinical trials for your site.
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.
Marketing and Advertising – Promoting your research site to attract participants.
Regulatory Management – Handling all regulatory documentation and compliance.
Patient Recruitment – Assisting with strategies to recruit and retain study participants.
Study Data Management – Managing and reporting all study data accurately.
Safety Data Management – Ensuring participant safety throughout the trial.
Invoicing – Handling study-related billing and financial management.
Staff Training – Training your in-office staff on clinical trial procedures.
Study Close-Out – Managing all necessary steps for successful trial completion.
Query Resolution – Resolving any queries that arise during the trial.
Drug Accountability – Tracking and managing study medications.
Storage and Archiving – Safely storing and archiving study materials for future reference.
