Category One
- Nexus Clinical Research
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- Category One
Active Studies
Alzheimer's Disease
Migraine
Atopic Dermatitis
Hypoparathyroidism
Upcoming Studies
Don’t See a Study That Matches Your Condition?
Whether you have a specific medical condition or are a healthy volunteer, you may still qualify to participate in a clinical research study.
Frequently Asked Questions
Find quick answers to the most common questions about our services, policies, and processes. If you don’t see what you’re looking for, feel free to contact us
Our site has access to a growing database of more than 20,000 pre-identified participants, supported by strong physician referral networks and targeted recruitment strategies. In addition, our location in South Florida provides access to a diverse patient population, including a large bilingual Hispanic community.
Nexus Clinical Research operates as a multi-specialty clinical trial site with experienced investigators in neurology, pulmonology, endocrinology, dermatology, cardiology, and internal medicine. This broad coverage allows our team to support a wide range of protocols and indications across Phase I–IV studies.
Our modern clinical research center includes:
Multiple dedicated exam rooms
Secure investigational product storage with temperature monitoring
Laboratory space for specimen processing
Private monitoring rooms for sponsor and CRO visits
Secure systems for data handling and regulatory documentation
This infrastructure allows us to support complex study protocols while maintaining a comfortable participant experience.
Clinical trials have specific eligibility requirements that must be met. This criteria varies and may include such factors as age, gender, the type and stage of a disease and previous medical treatment history. Some research studies seek participants with specific illnesses or medical conditions while others seek healthy participants.
You are free to end your participation in a trial at any time. Early study termination procedures will be performed to ensure your safe exit from the study.
Through our investigator network, Nexus Clinical Research has participated in 50+ completed clinical studies across multiple therapeutic areas. Our team has experience working with sponsors, CROs, and academic research organizations on a wide variety of protocols.
No medical insurance is required. All medical research services and study related materials are provided at no cost.
Our team follows strict GCP and HIPAA compliance standards. Staff members receive ongoing training, and our processes are designed to ensure accurate documentation, timely query resolution, and proactive monitoring of protocol adherence.
Clinical trials are research studies that explore whether a medical strategy, treatment, or device is safe and effective for humans. These studies also may show which medical approaches work best for certain illnesses or groups of people. Once a new drug has been evaluated and is found to be safe and effective, it may be approved by the FDA for doctors to prescribe.
Nexus Clinical Research is structured for rapid start-up timelines.
Typical activation benchmarks include:
Regulatory submissions: 3–5 business days
Budget & contract turnaround: 5–7 business days
Rapid feasibility completion
Our experienced regulatory and operations team ensures efficient study activation while maintaining strict compliance standards.
Millions of volunteers participate in industry-sponsored clinical trials each year. Medical researchers, doctors, and other health care professionals conduct these clinical research studies according to strict rules set by the Food and Drug Administration (FDA) to protect clinical trial volunteers. Despite, the possible benefits of participating in a clinical trial, volunteers also face the possible risk that the experimental treatment may not be effective and or that there may be unpleasant or serious side effects.
- ClinicalTrials.gov – English and Spanish www.clinicaltrials.govTelephone: 1-800-411-1222
- Food and Drug Administration (FDA) www.fda.govTelephone: 1-888-463-6332
Sponsors choose Nexus because of our combination of:
Access to a large and diverse patient population
Engaged and experienced investigators
Efficient study start-up timelines
Strong regulatory oversight
Reliable patient enrollment and retention strategies
Our goal is to deliver high-quality data while helping sponsors move their studies forward efficiently.
Clinical trial volunteers participate in the development of medical therapies that may offer better treatments and even cures for life-threatening and chronic diseases. Possible benefits for volunteers include:
- The opportunity to play an active role in your health care and gain a greater understanding of your disease or medical condition.
- Health assessments related to the study from our board-certified specialists.
- Study related medication and lab assessments at no cost.
- Access to promising new treatments often not available outside the clinical trial setting.
- Help others by contributing to medical research.
You should obtain as much information as possible before deciding to participate in a clinical trial. You should also feel comfortable asking the following questions and discussing any issues or concerns with your clinical research team members:
- What is the purpose of the clinical trial?
- Why do researchers believe the new treatment being tested may be effective?
- Has the treatment been tested before?
- What kinds of tests and treatments are involved?
- What are the possible study side effects and benefits?
- How might this trial affect my daily life?
- How long will the trial last?
- Will hospitalization be required?
- Who will pay for the treatment?
- Will I be reimbursed for expenses?
Yes. Sponsors and CROs may contact our team to request additional materials such as:
Site capabilities overview
Principal Investigator CVs
Recruitment strategy details
Feasibility assessments
Our team is available to discuss upcoming study opportunities and potential collaborations.