Sponsor-focused clinical operations partner
Carum Research - Clinical Trials and Medical Technology Evaluation

Sponsor-Focused Clinical Trials & Medical Technology Research

Pharmaceutical & Biologic Trials

Infrastructure supporting infusion therapies, biologics, and advanced pharmaceutical development.

Clinical validation and evaluation of devices, diagnostics, and digital health solutions.

Protocol-driven studies evaluating non-pharmacologic, interventional, and care-delivery models.

FOCUS AREAS

CNS & Rare Disease Research

We began with CNS and rare disease infrastructure and are ready for aligned partnerships across additional therapeutic areas.

Neurology
  • Multiple Sclerosis
  • Dementia
  • Myasthenia Gravis
  • Parkinson's
  • Epilepsy
  • AIDP/CIDP
Rare Diseases
  • Angelman Syndrome
  • NMO
Medical Technologies and Expanding Scope
  • Implantable devices
  • Wearable devices
  • Expanding scope to all medical subspecialties
Quality

Operational Infrastructure

A straightforward process designed to reduce operational noise and increase confidence in the dataset.

Fast feasibility responses with transparent operational constraints and enrollment assumptions.

  • Population fit, competing studies, and visit burden review
  • Operational resourcing plan and start-up timeline
  • Risk flags surfaced early (procedures, equipment, staffing)

Structured start-up checklists and role clarity before first subject in.

  • Protocol-specific training + documentation
  • Source templates and visit workflow mapping
  • Communication cadence established (weekly touchpoints as needed)

Tight visit execution, safety diligence, and rapid issue resolution.

  • Pre-visit confirmation + checklist-driven visits
  • Deviation prevention mindset; immediate corrective actions
  • Clear, timely sponsor/CRO communication

Monitoring-friendly documentation and audit-ready organization throughout the study lifecycle.

  • Source and essential document consistency
  • Query responsiveness and documentation discipline
  • Closeout planning from day one
Compliance-minded posture

We aim for sponsor expectations: documentation discipline, consistent workflows, and secure handling of sensitive data.

Designed for ICH-GCP-aligned documentation workflows
Quality and documentation patterns designed to align with GCP expectations.
Digital compliance-aware systems
Tools and processes selected with security and auditability in mind.
Privacy-forward posture
Operational controls intended to support HIPAA-conscious handling of PHI.
FAST LINKS
Technology

Medical Technology & Device Evaluation

Clinical Validation & Translation

Supporting the transition of therapeutic and medical technology innovations into disciplined clinical evaluation.

Medical Technology Research Platform

Infrastructure supporting the development, validation, and clinical evaluation of emerging medical technologies and digital health solutions

Innovation Partnerships

Collaborating with emerging and established sponsors to advance therapeutic and medical technology innovation.

Privacy-forward Documentation discipline Auditability-aware
Leadership
Experienced operators and clinical oversight.

A leadership team that includes more than 15 years of experience aligned to sponsor outcomes: speed, quality, and responsiveness.

Christina Howell - CEO of Carum Research
Christina Howell
CEO
Execution & Operations
Puneet Gupta, MD - CSIO of Carum Research
Puneet Gupta, MD
CSIO
Strategy & Innovation
Duc Tran, MD - CMO of Carum Research
Duc Tran, MD
CMO
Clinical Quality & Medical Leadership
Macym Rizvi, MD - Treasurer of Carum Research
Macym Rizvi, MD
Treasurer
Board & Executive Leadership
Partners

Why Sponsors Partner with Carum

We collaborate with established clinical and research organizations to expand capability and reach.

Trusted collaborations
Contact
Let's talk feasibility.

Drop us a quick message - we'd love to talk.

Sponsor inquiries

If you're a sponsor, CRO, or innovation partner, we can share our capability overview, typical timelines, and how we operationalize quality.

info@carumresearch.com
Dallas, Texas
PREFERRED FIRST MESSAGE
  • Protocol synopsis (or therapeutic area + phase)
  • Target timelines and enrollment goals
  • Key procedures + visit burden
  • Monitoring cadence / data expectations