Sponsors | CROs | Valiance Research

Sponsors
& CROs

Transformative Research

Collaborating with clients, Valiance conducts clinical studies across all phases of research and discovery, development, validation and approval. We add value across the full spectrum of clinical trials from fast and easy startups, dedicated recruitment staff for quick enrollment and retention, to capturing, reporting, and entering valuable data across applicable data capture systems.

Turn insight into impact

We are dedicated to upholding the highest quality standards at all our locations and throughout every clinical trial and working closely with partners to ensure that their therapies reach patients more quickly—one trial at a time. Valiance Clinical Research offers a capability framework designed to inform the fundamental requirements for clinical trial development while ensuring adherence to data quality and subject safety. To that end, our capacity and capabilities encompass the following:

Flexible | Scalable

Phase 1 - Phase 4 clinical trials
Full Time Board Certified Physicians
Full Time Board Certified Nurse Practitioners
Full Time Clinical Research Coordinators
Double locked, secured and monitored I.P and Document storage
Medical Imaging Capabilities - Ultrasound, X-Ray, CT-Scan, Endoscopy and more
Dedicated Monitoring Space

Secure | Controlled

Calibrated/Secured -70°c Freezers
Calibrated/Secured -20°c Freezer
Calibrated/Secured 2-8°c Refrigerator
Calibrated/Secured Ambient storage
Calibrated Ambient and refrigerated centrifuge
24/7 Current/Min/Max Investigational Product and sample temperature monitoring
Calibrated Blood Pressure Monitoring Devices
Calibrated Electrocardiogram Machines

Accessible | Equipped | Patient-Centered

Multiple Private Patient Rooms
Private Conference Rooms
Secure and Encrypted Wifi, Fax, Copy, Printer, and Scanners for Sponsor/CRO use
Dedicated Monitoring Space
Uber Health for Patient Transportation
Subject stipends distributed immediately after each completed visit via visa cards
Flexible schedules, including after hours and weekends
Bilingual staff, including, but not limited to: Spanish, Tagalog, Farsi, Cantonese, Korean, Armenian and English.

Study Start Up Process

The clinical trial start-up process is complex and involves coordination among various stakeholders, including sponsors, investigators and regulatory bodies. It is essential to follow rigorous procedures to ensure the safety and efficacy of new medical interventions. Valiance Clinical Research takes a proactive approach to clinical trial start-up and planning to avoid costly delays and maximize your chance of success

01.

CDA 2-3 Days

02.

Feasibility Questionaire 2-4 Days

03.

Budget/Contract/Regulatory All Done in Parallel

4-6 weeks

04.

Site activation 8-12 Weeks From the Time of CDA

05.

First Patient Screened 24-48hrs from activation

Reach. Retention. Results.

It is important that culturally and linguistically diverse people have access to clinical research to ensure that the evidence gathered is applicable to them. We know that there are potential factors such as racial differences in opioid receptors, cultural expression of pain, interaction with healthcare professionals, perception of interventions or hospital admission that may impact this. This is why it’s critical to have diverse representation in clinical trials – to better understand patient differences that may affect clinical outcomes. Our patient demographics consist of the following:

46.9%

Hispanic or Latino: 46.9% of the population

28.9%

White (non-Hispanic): 28.9% of the population

11.7%

Asian: 11.7% of the Local population

11.7%

African American: 8.3% of the population

3.3%

Two or more races: 3.3% of the population

0.7%

Other: 0.7% of the local population

Advancing Therapeutics, Transforming Outcomes

Failure to meet enrollment targets or population diversity can compromise data quality and regulatory acceptance. Our sites achieve a 97% retention rate through frequent check-ins, text reminders, and personalized engagement. We meet 98% of enrollment goals, with 80% from internal databases, 10% from referrals, 5% from community events, and 5% from digital marketing.

Targeted Solutions to Enhance Patient Care

We utilize our deep medical expertise and insights into gaps in patient care to help develop cutting-edge therapies and innovative solutions. By focusing on essential therapeutic areas, we aim to address complex diseases and expand treatment options, ultimately enhancing patient outcomes and improving quality of life. These therapeutic areas are the following:

Cardiology

Neurology

Dermatology

Rheumatology

Gastroenterology

Hepatology

Pulmonology

Nephrology

Endocrine and Metabolic Diseases

Internal and Family Medicine

Multidisciplinary Professionals

Valiance Clinical Reasearch has a well-established and experienced research team of Doctors, Nurses, Laboratory and support staff all dedicated to producing quality research.

Meet Our Team

Our expert teams work closely with sponsors to tailor the best solution for each project.

Meet Our Team

Sponsor A Study

We have expertise in conducting clinical trials and the efficacy of treatment for a wide range of conditions.

Request A Proposal

Brands We Have Worked With

Brands We Have Worked With To Drive Incredible Clinical Results

Bringing a wealth of experience to study design, recruitment and execution.

OFFICIAL

About

Valiance Clinical Research combines expertise, agility, and proactive strategies to optimize clinical development and help deliver impactful therapies to patients