Setting the Standard

Performance, Quality, and Experience

These are the distinctive hallmarks that define our clinical research company. Discover the reasons why we truly stand out from the rest in the highly competitive industry. Our commitment to excellence and innovation sets us apart, ensuring that we provide unparalleled service and results.

Driving Excellence in Clinical Research Partnership

Proven Track Record of Success

Our site has a history of exceeding recruitment targets and delivering high-quality data, ensuring reliable and efficient study outcomes.

Diverse Therapeutic Expertise

With a focus on various therapeutic areas, including pulmonology, our experienced team provides comprehensive support across multiple fields of research.

Diverse Patient Population Access

Located in South Florida, we offer access to a diverse and engaged patient population, enhancing the generalizability and applicability of study results.

Strong Community Relationships

Our established connections with local healthcare providers and community organizations facilitate smooth patient recruitment and retention.

Experienced Research Team

Our skilled team of researchers is committed to maintaining the highest standards of quality and integrity in every study.

Commitment to Innovation

We embrace cutting-edge technologies and methodologies to streamline clinical trial processes, ensuring that sponsors benefit from efficient and innovative solutions.

Therapeutic Experience

View Our Comprehensive List of Therapeutic Areas to Explore the Extensive Depth of Experience and Expertise That Our Clinical Research Network Brings to Your Study.

Cardiovascular Disease

Asthma

Hypertension

Obesity

Irritable Bowel Syndrome

Dementia

Women’s Health

COPD

Weight Loss

Ulcerative Colitis

Diabetes Mellitus

Vaccine

Osteoporosis

Hyperlipidemia

Osteoarthritis

Rheumatoid Arthritis

Alzheimer’s Disease

Migraines

Crohn's Disease

Anemia

  • Includes automatic calculation for precise cardiac monitoring.

    • -20°C freezer for general storage needs.

    • -70°C freezer, with the ability to ship samples same-day on dry ice.

    • -80°C freezer for long-term storage.

    • 2°C to 8°C refrigerator for temperature-sensitive materials.

    • Backup -20°C freezer for emergency storage.

    • Ambient centrifuge with ice bath for versatile sample processing.

    • Ambient storage for non-temperature-sensitive materials.

  • Continuous monitoring for IP storage, with access to backup power through a generator or SOP for power failure.

Advanced Equipment and Facilities

Imaging and Diagnostic Capabilities

    • Coronary Computed Tomography Angiography (CCTA)

    • CT scan

    • Echocardiogram

    • MRI/CT/PET, onsite or nearby

    • Spirometry with experience conducting tests according to ATS-2019 Guidelines

    • FeNO and Forced oscillatory technique

    • 12-Lead ECG: Includes automatic calculation for precise cardiac monitoring.

    • Holter Monitoring: Continuous 24-hour heart monitoring for arrhythmia detection.

    • Stress Testing: Cardiac stress tests to evaluate heart performance under exertion.

    • Bone Density Scans (DEXA): Dual-energy X-ray absorptiometry for assessing bone health.

    • Oxygen Saturation Monitoring: Continuous pulse oximetry for patient monitoring.

    • Documented disaster/pandemic business continuity plan

    • GCP compliant record storage

    • Electronic Medical Records (EMR)

    • Computer and Wi-Fi connection

    • Ability to enroll 25% or more Black/African-American patients

    • Prompt data entry

    • Patient-reported outcome assessments

    • Willingness to partner with home health for study visits

    • Ability to refer to other specialty physicians

Operational and Support Features

Striving for Continual Improvement: Our Dedication to Progress and Growth

We perform internal study audits on a regular basis.

  • Review study protocols, EDC screen shots, and source documents to ensure that the source accurately and completely reflects the protocol’s requirements and site’s documentation requirements

  • Review completed source documents for accuracy, completeness, and legibility

  • Compare data in source documents to data transcribed in EDC for accuracy

  • Identify trends in errors to initiate improvements in source document flow, collection, and site processes

  • Review regulatory binders for proper organization, filing, delegation of authority, documentation, and completeness of training

  • Review site processes and forms and suggest revisions that will make the collection of data more streamlined

Adherence to these established processes, in combination with the rigorous FDA guidelines for research and well-defined good clinical practices, is ultimately what drives Pioneer Clinical Studies (PCS) to consistently evolve, improve, and efficiently deliver your company with high-quality data that is both reliable and actionable.

Join Our Clinical Trials Today.

Are you interested in accessing the latest and most innovative treatments available within your local community? By participating in our clinical trials, you can not only benefit from cutting-edge therapies but also contribute significantly to the advancement of healthcare for everyone. Simply fill out our eligibility form, and one of our dedicated and knowledgeable recruiters will reach out to you shortly to discuss your potential participation and answer any questions you may have.