Partner with chroniclebio for Clinical Trial Excellence

We partner with specialty clinics already treating thousands of neuroimmune patients, ensuring rapid trial recruitment, diverse cohorts, and clinically validated endpoints.

Why Choose Our Site?

With sites in Texas, Utah, Arizona, and India we are a trusted partner offering centralized support from IRB submissions to budgeting and contracting. We’re invested in your success and the rapid advancement of research.

20,000+
Patients With
Complex Conditions
4
Weeks Site Selection
to Activation
6
Therapeutic
Areas
3x
Trial Top
Enroller

We connect trials to those who need answers most and the specialty clinics serving patients with complex conditions often forgotten in medicine.

THERAPEUTIC AREAS

CARDIOLOGY

Postural orthostatic tachycardia syndrome (POTS), Inappropriate sinus tachycardia (IST), Hypertension, Heart failure (HFpEF and HFrEF), Atrial fibrillation, Heart failure, Hypotension

ALLERGY & IMMUNOLOGY

Long COVID (post-viral syndrome), Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), Mast cell activation syndrome (MCAS), Asthma, Eczema/atopic dermatitis

NEUROLOGY

Migraine & chronic migraine, Cluster headache, Post-traumatic headache, Menstrual-related migraine, Idiopathic intracranial hypertension (IIH), Intracranial hypotension

GENETIC & METABOLIC

Connective tissue disorders (e.g., Ehlers-Danlos syndrome, Marfan), Mitochondrial disorders, Cardiovascular conditions, Metabolic and hormone disorders

GENERAL MEDICINE

Dysautonomia, Hyperlipidemia (high cholesterol), Diabetes & pre-diabetes, Obesity/weight management, Thyroid Disorders, Hormone & metabolic changes, Sjogren’s syndrome

FAMILY MEDICINE

Gastroesophageal reflux disease (GERD), Small intestinal bacterial overgrowth (SIBO), Irritable bowel syndrome (IBS), Thyroid disorders, Atopic dermatitis (Eczema)

Reliable Data & Compliance

We adhere to strict industry standards, delivering accurate and high-quality data on which you can rely. As a high-enrolling site, we maintain constant audit and inspection readiness, providing peace of mind for sponsors and CROs.

Personalized Collaboration

We create tailored solutions to meet the unique needs of every sponsor and study. Our flexible approach ensures your priorities are met with precision, and we remain responsive and adaptable throughout every phase of the trial.

Experienced Research Team

Our team brings extensive experience in clinical research and regulatory compliance. Over the years, we have forged strong relationships with sponsors and CRO partners, ensuring a collaborative and efficient approach to every trial.

Rapid Site Activation

We minimize delays to keep your trial on schedule. Our sites can be activated within 4-6 weeks of selection. Our team works diligently to quickly screen and enroll participants, accelerating the timeline to meet your goals.

High Enrollment & Retention

We have established proven processes with patient acquisition recruitment strategies. We prioritize participant well-being and foster a compassionate environment, ensuring high satisfaction and engagement throughout the trial.

State-of-the-Art Facilities

Our research sites in TX, AZ, UT, and India feature modern labs and the latest technology to support a wide range of trials. Sponsors choose us because of our commitment to participants and consistency as a top enrolling site.

CHRONICLEBIO capabilities

    • Dedicated clinical research suites

    • Private exam rooms with monitoring capabilities

    • Infusion and observation bays

    • Sample collection and processing room

    • Temperature-controlled specimen storage areas

    • ADA-accessible facilities

    • Secure document storage (GCP compliant)

    • Patient lounge with Wi-Fi and refreshments

    • On-site phlebotomy and vitals stations

    • ECG/EKG machines

    • Spirometry and pulmonary function testing

    • Centrifuges (refrigerated and standard)

    • Refrigerators and freezers (-20°C and -80°C)

    • Portable vital sign monitors

    • Digital scale and stadiometer

    • Infusion pumps

    • iPads/tablets for ePRO and survey data

    • Barcode scanners and sample tracking software

    • Backup generators for critical equipment

    • Board-certified principal investigators (multi-specialty)

    • Clinical research coordinators (GCP certified)

    • Phlebotomists and lab technicians

    • Registered nurses with infusion experience

    • Regulatory specialists and QA oversight

    • Data managers and eCRF experts

    • Experienced in Phase I–IV protocols and observational studies

    • On-site -20°C and -80°C freezers

    • Real-time temperature monitoring with alert systems

    • Chain of custody tracking and sample logging

    • Long-term sample storage capabilities

    • IATA-certified staff for compliant sample shipping

    • Aliquoting and labeling with barcoding

    • Integration with digital LIMS systems

    • Consent-compliant specimen archiving

    • Dedicated space for genomic and biomarker sample processing

    • BioReference Laboratories (diagnostic and research support)

    • In-house CLIA-waived testing capabilities

    • Strong relationships with national courier services

    • Integrations with EDC and EMR for seamless lab result upload

Let’s connect about your next trial

Contact us today to learn how we can advance your clinical trial success.