Trevion Clinical Research

— Your trusted site partner in clinical trials

Comprehensive site‑level support. Efficient execution. Exceptional integrity.

Your Trusted Site Partner in Clinical Trials

Trevion Clinical Research is a Site Management Organization (SMO) committed to delivering excellence at the site level. We partner with sponsors, CROs, and investigators to provide efficient, compliant, and patient‑centered clinical trial support.

Our goal is to streamline site operations and accelerate study performance with integrity, accuracy, and transparency.

Key Value Propositions

  • Operational excellence and GCP‑compliant systems
  • Rapid site activation and startup
  • Strong patient recruitment and retention strategies
  • Experienced CRCs and clinical staff
  • Audit‑ready documentation and quality oversight
  • Scalable support for Phase I–IV and hybrid trials

Your Trusted Site Partner in Clinical Trials

Trevion Clinical Research is a Site Management Organization (SMO) committed to delivering excellence at the site level. We partner with sponsors, CROs, and investigators to provide efficient, compliant, and patient‑centered clinical trial support.

Our goal is to streamline site operations and accelerate study performance with integrity, accuracy, and transparency.

Key Value Propositions

  • Operational excellence and GCP‑compliant systems
  • Rapid site activation and startup
  • Strong patient recruitment and retention strategies
  • Experienced CRCs and clinical staff
  • Audit‑ready documentation and quality oversight
  • Scalable support for Phase I–IV and hybrid trials

Discover why sponsors and CROs choose us as their strategic site-level partner for predictable, high-quality execution.

Services

Why Sponsors & CROs Partner With Trevion

Why Choose Us

  • Proven Reliability

    Consistent, dependable operations backed by strong SOPs and transparent workflows.

  • Efficiency & Speed

    Rapid study startup, accelerated recruitment, and fast turnaround times.

  • Reduced Site Burden

    We manage regulatory, operational, and data responsibilities so investigators can focus on patient care.

  • Flexible, Scalable Models

    Support for any phase, therapeutic area, or site volume with adaptable service models.

  • Partnership‑Driven Support

    We operate as an extension of sponsor and CRO teams, ensuring seamless communication and aligned goals.

  • Ethical & Patient‑Centered

    We uphold patient safety, informed consent, and regulatory excellence as core priorities.

Therapeutic Areas

Supported Therapeutic Areas
  • Metabolic Disorders
  • Cardiovascular
  • Gastrointestinal
  • Pulmonology
  • Behavioral & Neurological Health
  • Oncology (site dependent)

Capability Statement

Core Competencies
  • Full‑service site management
  • Regulatory documentation & oversight
  • Trained CRCs and clinical support staff
  • Patient recruitment & retention
  • Data management and quality review
  • Hybrid & decentralized trial support
Value Delivered
  • Faster startup timelines
  • Improved enrollment performance
  • Reduced operational burden for sites
  • Strong protocol compliance
  • Enhanced sponsor‑site relationships
Commitment

We prioritize data integrity, patient safety, compliance, and transparent communication at every stage of the clinical trial.